Supporting Information:

Similar documents
pyrazoles/isoxazoles library using ketene dithioacetals

Supporting Information

Poly(4-vinylimidazolium)s: A Highly Recyclable Organocatalyst Precursor for. Benzoin Condensation Reaction

Synthesis of Trifluoromethylated Naphthoquinones via Copper-Catalyzed. Cascade Trifluoromethylation/Cyclization of. 2-(3-Arylpropioloyl)benzaldehydes

Regioselective Synthesis of 1,5-Disubstituted 1,2,3-Triazoles by reusable

Solvent-controlled selective synthesis of biphenols and quinones via oxidative coupling of phenols

An Efficient Total Synthesis and Absolute Configuration. Determination of Varitriol

Hualong Ding, Songlin Bai, Ping Lu,* Yanguang Wang*

Supporting Information

Supporting Information

Supporting Information

Supporting Information

*Corresponding author. Tel.: , ; fax: ; Materials and Method 2. Preparation of GO nanosheets 3

Synthesis of Dihydroquinoline Based Merocyanines as Naked Eye and Fluorogenic sensors for Hydrazine Hydrate in Aqueous Medium

Supporting Information

Supporting Information

Diaza [1,4] Wittig-type rearrangement of N-allylic-N- Boc-hydrazines into -amino-n-boc-enamines

A Mild, Catalytic and Highly Selective Method for the Oxidation of α,β- Enones to 1,4-Enediones. Jin-Quan Yu, a and E. J.

Brønsted Base-Catalyzed Reductive Cyclization of Alkynyl. α-iminoesters through Auto-Tandem Catalysis

Nanocrystalline Magnesium Oxide-Stabilized Palladium(0): An Efficient and Reusable Catalyst for the Synthesis of N-(2- pyridyl)indoles

Supporting Information for Synthesis of C(3) Benzofuran Derived Bis-Aryl Quaternary Centers: Approaches to Diazonamide A

N-Hydroxyphthalimide: a new photoredox catalyst for [4+1] radical cyclization of N-methylanilines with isocyanides

Supporting Information

Supporting Information

Supplementary Material (ESI) for Organic & Biomolecular Chemistry This journal is (c) The Royal Society of Chemistry Supplementary data

SUPPLEMENTARY INFORMATION

Effect of Conjugation and Aromaticity of 3,6 Di-substituted Carbazole On Triplet Energy

Supporting Information

Tsuji Trost N-Allylation with Allylic Acetates by Using a Cellulose Palladium Catalyst

Divergent Synthesis of CF 3 -Substituted Polycyclic Skeletons Based on Control of Activation Site of Acid Catalysts

Carbonylative Coupling of Allylic Acetates with. Arylboronic Acids

Supporting information for A simple copper-catalyzed two-step one-pot synthesis of indolo[1,2-a]quinazoline

for Brønsted Base-Mediated Aziridination of 2- Alkyl Substituted-1,3-Dicarbonyl Compounds and 2-Acyl-1,4-Dicarbonyl Compounds by Iminoiodanes

SYNTHESIS OF A 3-THIOMANNOSIDE

Silver-catalyzed decarboxylative acylfluorination of styrenes in aqueous media

Efficient Pd-Catalyzed Amination of Heteroaryl Halides

Domino reactions of 2-methyl chromones containing an electron withdrawing group with chromone-fused dienes

Electronic Supplementary Information. A novel generation of hybrid photochromic. through fine-tuning of surface chemistry

Hai-Bin Yang, Xing Fan, Yin Wei,* Min Shi*

Palladium-Catalyzed Oxidative Cyclization of Tertiary Enamines for Synthesis of 1,3,4-Trisubstituted Pyrroles and 1,3-Disubstituted Indoles

Tetrahydrofuran (THF) was distilled from benzophenone ketyl radical under an argon

Supporting Information

Supporting Information

Fast and Flexible Synthesis of Pantothenic Acid and CJ-15,801.

An efficient one pot ipso-nitration: Structural transformation of a dipeptide by N-terminus modification

Room Temperature N-Arylation of Amino Acids and Peptides Using Copper(I) and β-diketone

Supporting Information

A Facile and General Approach to 3-((Trifluoromethyl)thio)- 4H-chromen-4-one

Supporting Information

Halogen halogen interactions in diiodo-xylenes

Supplementary Information

Amide Directed Cross-Coupling between Alkenes and Alkynes: A Regio- and Stereoselective Approach to Substituted (2Z,4Z)-Dienamides

Synthesis and Use of QCy7-derived Modular Probes for Detection and. Imaging of Biologically Relevant Analytes. Supplementary Methods

Bio-based Green Solvent Mediated Disulfide Synthesis via Thiol Couplings Free of Catalyst and Additive

Singapore, #05 01, 28 Medical Drive, Singapore. PR China,

Supporting Information

Supplementary information

The First Asymmetric Total Syntheses and. Determination of Absolute Configurations of. Xestodecalactones B and C

Supporting Information

Tuning Porosity and Activity of Microporous Polymer Network Organocatalysts by Co-Polymerisation

Supporting Information. DBU-Mediated Metal-Free Oxidative Cyanation of α-amino. Carbonyl Compounds: Using Molecular Oxygen as the Oxidant

Supporting Information

Supporting Information. Sandmeyer Cyanation of Arenediazonium Tetrafluoroborate Using Acetonitrile as Cyanide Source

A new route for the synthesis of highly substituted 4- aminoquinoline drug like molecules via aza hetero-diels-alder reaction

Supporting Information. Contents

How to build and race a fast nanocar Synthesis Information

Enantioselectivity switch in copper-catalyzed conjugate addition. reaction under influence of a chiral N-heterocyclic carbene-silver complex

SUPPORTING INFORMATION

Supporting Information. A rapid and efficient synthetic route to terminal. arylacetylenes by tetrabutylammonium hydroxide- and

Supporting Information

Scalable Synthesis of Fmoc-Protected GalNAc-Threonine Amino Acid and T N Antigen via Nickel Catalysis

Supporting Information for

Enantioselective Conjugate Addition of 3-Fluoro-Oxindoles to. Vinyl Sulfone: An Organocatalytic Access to Chiral. 3-Fluoro-3-Substituted Oxindoles

Electronic Supplementary Information

Supplementary Information. Mapping the Transmission Function of Single-Molecule Junctions

Supporting Information - I: Experimental Procedures and Characterization

Dual role of Allylsamarium Bromide as Grignard Reagent and a. Single Electron Transfer Reagent in the One-Pot Synthesis of.

Supporting Information:

Electronic Supporting Information

O-Allylation of phenols with allylic acetates in aqueous medium using a magnetically separable catalytic system

Aziridine in Polymers: A Strategy to Functionalize Polymers by Ring- Opening Reaction of Aziridine

Iridium-catalyzed regioselective decarboxylative allylation of. β-ketoacids: efficient construction of γ, δ-unsaturated ketones

Iron Catalyzed Cross Couplings of Azetidines: Application to an Improved Formal Synthesis of a Pharmacologically Active Molecule

Supporting Information for: Synthesis of Chiral Tryptamines via a Regioselective Indole Alkylation

Supporting Information. Efficient N-arylation and N-alkenylation of the five. DNA/RNA nucleobases

Electronic Supplementary Information for New Journal of Chemistry

Supporting Information

A TTFV pyrene-based copolymer: synthesis, redox properties, and aggregation behaviour

Supplementary Information. Novel Stereocontrolled Amidoglycosylation of Alcohols with Acetylated Glycals and Sulfamate Ester

Supporting Information

Electronic Supplementary Information for. A Redox-Nucleophilic Dual-Reactable Probe for Highly Selective

Aminoacid Based Chiral N-Amidothioureas. Acetate Anion. Binding Induced Chirality Transfer

Electronic Supplementary Information

Direct Synthesis of Pyrazoles from Esters using tert-butoxide-assisted C-(C=O) Coupling

Simplified platensimycin analogues as antibacterial agents

Synthesis of Secondary and Tertiary Amine- Containing MOFs: C-N Bond Cleavage during MOF Synthesis

Supporting Information for: Direct Conversion of Haloarenes to Phenols under Mild, Transition-Metal-Free Conditions

Supporting Information for: Phosphonates

Supporting Information

Highly Efficient Chemoselective N-TBS Protection of Anilines under Exceptional Mild Conditions in the Eco-Friendly Solvent 2- Methyltetrahydrofuran.

Transcription:

Electronic Supplementary Material (ESI) for Green Chemistry. This journal is The Royal Society of Chemistry 2016 Supporting Information: A metal free reduction of aryl-n-nitrosamines to corresponding hydrazines using sustainable reductant thiourea dioxide Priyanka Chaudhary a, Surabhi Gupta a, Popuri Sureshbabu b, Shahulhameed Sabiah b and Jeyakumar Kandasamy a* a Department of chemistry, Indian Institute of Technology (BHU), Varanasi, Uttar Pradesh-221005; Email: jeyakumar.chy@iitbhu.ac.in b Department of chemistry, Pondicherry University, Pondicherry-605014 S No List of contents: Page No 1 General information 2 2 Experimental procedure for the reduction of N-nitrosamines 2 3 Experimental procedure for the one pot synthesis of N,N- disubstituted hydrazines 4 Experimental procedure for the reduction of N-nitroso diaryl amine 2 3 5 Analytical data of the products 3 6 1 H and 13 C NMR Spectrum of N,N-disubstituted hydrazines 11-33 1

1. General information All the reactions were performed in round bottom flask at appropriate temperature mentioned in the manuscript. Solvents and chemicals were purchased from commercial sources and used without further purifications. Thin layer chromatography was performed using pre-coated plates obtained from E. Merck (TLC silica gel 60 F 254 ). The NMR spectra were recorded on Bruker Avance 500 MHz NMR spectrometer and/or Bruker Avance 400 MHz in CDCl 3 Solvent. Mass spectra (HRMS) were measured on water s Quattro Micro V 4.1. The purification of the products were performed on silica gel (60-120 mesh) using a mixture of ethyl acetate and hexane. All the products were characterized by proton and carbon NMR as well as mass spectrometry. In proton NMR, TMS is calibrated to 0 ppm and in 13 C NMR CDCl 3 peak is calibrated to 77.0 ppm. 2. Experimental procedure for the reduction of N-nitrosamines N-nitrosamine (1.0 mmol) was allowed to stir in methanol (2 ml) approximately for 5 min at 50 o C to which aqueous solution of sodium hydroxide (1 M, 6 equiv.) followed by thiourea dioxide (TDO) (3 equiv.) was added. The reaction was allowed to stir for 3-4 h and the progress of the reaction was monitored by TLC. After completion, the reaction mixture was diluted with chloroform and washed with water. The organic layer was dried over anhydrous sodium sulphate, concentrated and subjected for column chromatography (SiO 2 : ethyl acetate/hexane) to obtain corresponding pure substituted N-aryl hydrazines. 3. Experimental procedure for the one pot synthesis of N,N-disubstituted hydrazines At the beginning, secondary amine (1 mmol) was converted to corresponding N- nitrosamine using 1.2 equiv. tert-butyl nitrite in 25 ml flask at room temperature to which methanol (2 ml) was added. Then the reaction mixture was kept at pre-heated oil-bath at 50 o C to which aqueous solution of sodium hydroxide (1 M, 6 equiv.) followed by thiourea dioxide (TDO) (3 equiv.) was added. The resulting mixture was allowed to stir for 4 h at same temperature. After completion, the reaction mixture was diluted with chloroform and washed with water. The organic layer was dried over anhydrous sodium sulphate, concentrated and subjected for column chromatography (SiO 2 : ethyl acetate/hexane) to obtain corresponding pure aryl hydrazine. 2

4. Experimental procedure for the reduction of N-nitroso dialkylamine: N-nitroso dibenzylamine (1.0 mmol) was allowed to stir in methanol (2 ml) approximately for 5 min at 50 o C to which aqueous solution of sodium hydroxide (1 M, 10 equiv.) followed by thiourea dioxide (TDO, 5. equiv.) was added. The reaction was allowed to stir for 6 h and the progress of the reaction was monitored by TLC. After completion, the reaction mixture was diluted with chloroform and washed with water. The organic layer was dried over anhydrous sodium sulphate, concentrated and subjected for column chromatography (SiO 2 : ethyl acetate/hexane) to obtain corresponding pure substituted N,Ndibenzyl hydrazine (2w). 5. Analytical Data of the Products 5.1 N-benzyl N-phenyl hydrazine (2a) was obtained as white solid (160 mg, 81%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.28 7.17 (m, 7H), 7.02 (d, J = 7.7 Hz, 2H), 6.74 (t, J = 7.3 Hz, 1H), 4.52 (s, 2H, Benzylic-CH 2 ), 3.47 (brs, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 151.7, 137.5, 129.0, 128.6, 127.8, 127.3, 118.5, 113.6, 60.3. HRMS: Calc. for C 13 H 14 N 2 [M+H] + : 199.1235, Obser.: 199.1226. 5.2 N-(4-methylbenzyl)-N-phenylhydrazine (2b) was obtained as yellow solid (180 mg, 78%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.27 7.22 (m, 2H), 7.18 (d, J = 7.8 Hz, 2H), 7.13 (d, J = 7.7 Hz, 2H), 7.09 (d, J = 8.1 Hz, 2H), 6.80 (t, J = 7.3 Hz, 1H), 4.53 (s, 2H, Benzylic-CH 2 ), 3.50 (brs, NH 2 ), 2.33 (s, 3H, aryl-ch 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 151.8, 137.0, 134.3, 129.3, 129.0, 127.9, 118.5, 113.7, 60.1, 21.0. HRMS: Calc. for C 14 H 16 N 2 [M+H] + : 213.1392, Obser.: 213.1385 5.3 N-(4-methoxybenzyl)-N-phenylhydrazine (2c) was obtained as white solid (173 mg, 76%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.26 (m, 2H), 7.22 (d, J = 8.4 Hz, 2H), 7.11 (d, J = 8.3 Hz, 3

2H), 6.87 (d, J = 8.4 Hz, 2H), 6.82 (t, J = 7.2 Hz, 1H), 4.52 (s, 2H, Benzylic-CH 2 ), 3.80 (s, 3H, Aryl-OCH 3 ), 3.49 (s, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 158.9, 151.7, 129.2 (2C), 129.0, 118.6, 114.0, 113.9, 59.8, 55.2. HRMS: Calc. for C 14 H 16 N 2 O [M+H] + : 229.1341, Obser.: 229.1332 5.4 N-(4-chlorobenzyl)-N-phenylhydrazine (2d) was obtained as white solid (186 mg, 80%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.23 7.14 (m, 6H), 6.96 (d, J = 7.7 Hz, 2H), 6.75 (t, J = 7.3 Hz, 1H), 4.47 (s, 2H, Benzylic-CH 2 ), 3.50 (brs, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 151.5, 136.2, 133.0, 129.1 (2C), 128.7, 118.8, 113.5, 59.7. HRMS: Calc. for C 13 H 13 ClN 2 [M+H] + : 233.0846, Obser.: 233.0835. 5.5 N-benzyl-N-(4-methylphenyl) hydrazine (2e) was obtained as white solid (165 mg, 78%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.34 7.27 (m, 5H), 7.07 (d, J = 8.2 Hz, 2H), 7.00 (d, J = 8.2 Hz, 2H), 4.52 (s, 2H, Benzylic-CH 2 ), 3.49 (brs, 2H, NH 2 ), 2.27 (s, 3H, CH 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 149.7, 137.6, 129.5, 128.6, 128.1, 128.0, 127.3, 114.1, 61.0, 20.3. HRMS: Calc. for C 14 H 16 N 2 [M+H] + : 213.1392, Obser. : 213.1382. 5.6 N-benzyl-N-(4-chlorophenyl) hydrazine (2f) was obtained as white solid (165 mg, 71%) 1 H NMR (500 MHz, CDCl 3 ) δ 7.34 (t, J = 7.3 Hz, 2H), 7.32 7.24 (m, 3H), 7.19 (d, J = 8.9 Hz, 2H), 7.03 (d, J = 8.6 Hz, 2H), 4.56 (s, 2H, Benzylic-CH 2 ), 3.53 (brs, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 150.3, 136.8, 128.8, 128.7, 127.8, 127.5, 123.2, 114.8, 60.2. HRMS: Calc. for C 13 H 13 ClN 2 [M+H] + : 233.0846, Obser. : 233.0833. 4

5.7 N-(4-bromobenzyl)-N-phenylhydrazine (2g) was obtained as white solid (207 mg, 75%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.36 7.27 (m, 5H), 7.26 (d, J = 7.4 Hz, 2H), 6.98 (d, J = 8.2 Hz, 2H), 4.57 (s, 2H, Benzylic-CH 2 ), 3.53 (s, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 150.6, 136.8, 131.7, 128.7, 127.7, 127.5, 115.2, 110.3, 60.0. HRMS: Calc. for C 13 H 13 BrN 2 [M+H] + : 277.0340, Obser. : 277.0333. 5.8 N-benzyl-(4-fluorophenyl) hydrazine (2h) was obtained as yellow solid (156 mg, 72%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.28 (t, J = 8.4 Hz, 2H), 7.24 7.21 (m, 3H), 7.04 6.96 (m, 2H), 6.88 (t, J = 8.7 Hz, 2H), 4.43 (s, 2H, Benzylic-CH 2 ), 3.41 (brs, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 156.6 (d, J C-F =237.5 Hz), 148.3, 148.3, 137.0, 128.7, 128.1, 127.5, 115.6 (d, J C-F =7.4 Hz), 115.3 (d, J C-F =22.2 Hz), 61.7. HRMS: Calc. for C 13 H 13 FN 2 [M+H] + : 217.1141, Obser.: 217.1145 5.9 N-benzyl-(2-methoxyphenyl) hydrazine (2i) was obtained as yellow liquid (157 mg, 69%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.36 7.29 (m, 4H), 7.29 (dd, J = 5.9, 2.9 Hz, 1H), 7.15 (dd, J = 8.1, 1.6 Hz, 1H), 7.06 7.01 (m, 1H), 6.95 6.90 (m, 2H), 4.31 (s, 2H, Benzylic-CH 2 ), 3.93 (s, 3H, OCH 3 ), 3.52 (brs, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 151.6, 141.9, 137.5, 129.1, 128.3, 127.3, 123.6, 120.8, 119.7, 111.3, 63.4, 55.5. HRMS: Calc. for C 14 H 16 N 2 O [M+H] + : 229.1341, Obser. : 229.1334. 5

5.10 N-(4-methoxybenzyl)-(4-chlorophenyl) hydrazine (2j) was obtained as pale brown solid (194 mg, 74%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.24 7.17 (m, 4H), 7.03 (d, J = 8.7 Hz, 2H), 6.86 (d, J = 8.2 Hz, 2H), 4.46 (s, 2H, Benzylic-CH 2 ), 3.79 (s, 3H, Aryl-OCH 3 ), 3.45 (s, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 159.1, 150.3, 129.2, 128.7, 128.6, 123.2, 115.1, 114.1, 59.6, 55.2. HRMS: Calc. for C 14 H 15 ClN 2 O [M+H] + : 263.0951, Obser.: 263.0947. 5.11 N-(4-chlorobenzyl)-(4-methylphenyl) hydrazine (2k) was obtained as pale yellow solid (185 mg, 75%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.21 (d, J = 8.2 Hz, 2H), 7.15 (d, J = 8.6 Hz, 2H), 6.99 (d, J = 8.0 Hz, 2H), 6.88 (d, J = 8.3 Hz, 2H), 4.41 (s, 2H, Benzylic-CH 2 ), 3.44 (s, 2H, NH 2 ), 2.20 (s, 3H, Aryl-CH 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 149.5, 136.3, 133.0, 129.6, 129.3, 128.7, 128.3, 114.0, 60.3, 20.3. HRMS: Calc. for C 14 H 15 ClN 2 [M+H] + : 247.1002, Obser.: 247.0990 5.12 N-(4-bromophenyl)-N-(4-methoxybenzyl) hydrazine (2l) was obtained as white solid (236 mg, 77%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.30 (d, J = 8.6 Hz, 2H), 7.16 (d, J =8.1 Hz, 2H), 6.97 (d, J = 8.4 Hz, 2H), 6.86 (d, J = 7.7 Hz, 2H), 4.47 (s, 2H, Bezylic-CH 2 ), 3.78 (s, 3H, Aryl- OCH 3 ), 3.45 (s, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 159.1, 150.7, 131.6, 129.2, 128.5, 115.5, 114.1, 110.4, 59.5, 55.2. HRMS: Calc. for C 14 H 15 BrN 2 O [M+H] + : 307.0446, Obser. : 307.0431. 6

5.13 N-(4-methylbenzyl)-(4-bromophenyl) hydrazine (2m) was obtained as yellow solid (229 mg, 79%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.16 (d, J = 9.0 Hz, 2H), 7.13 (s, 4H), 7.01 (d, J = 9.0 Hz, 2H), 4.49 (s, 2H, Bezylic-CH 2 ), 3.47 (s, 2H, NH 2 ), 2.32 (s, 3H, Aryl-CH 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 150.3, 137.2, 133.6, 129.4, 128.7, 127.8, 123.1, 114.9, 60.0, 21.0. HRMS: Calc. for C 14 H 15 BrN 2 [M+H] + : 291.0497, Obser.: 291.0491. 5.14 N-(4-chlorobenzyl)-N-4-methyl hydrazine (2n) was obtained as white solid (179 mg, 73%). 1 H NMR (500 MHz, CDCl 3 ) δ7.30 (d, J = 9.0 Hz, 2H), 7.14 (m, 4H), 6.97 (d, J = 9.0 Hz, 2H), 4.51 (s, 2H, Benzylic-CH 2 ), 3.49 (s, 2H, NH 2 ), 2.32 (s, 3H, Aryl-CH 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 150.3, 137.2, 133.6, 129.3, 128.7, 127.8, 123.1, 114.9, 60.2, 21.0. HRMS: Calc. for C 14 H 15 ClN 2 [M+H] + : 247.1002, Obser.: 247.0997 5.15 N-(4-bromophenyl)-N-(4-chlorobenzyl) hydrazine (2o) was obtained as white solid (234 mg, 76%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.31 7.25 (m, 4H), 7.18 (d, J = 6.3 Hz, 2H), 6.92 (d, J = 6.6 Hz, 2H), 4.52 (s, 2H, Benzylic-CH 2 ), 3.53 (s, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 150.4, 135.4, 133.3, 131.7, 129.0, 128.9, 115.2, 110.7, 59.5. HRMS: Calc. for C 13 H 12 BrClN 2 [M+H] + : 310.9951, Obser. : 310.9927 7

5.16 N-(4-methylbenzyl)-N-(4-methoxyphenyl) hydrazine (2p) was obtained as red liquid (169 mg,70%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.21 (m, 2H), 7.16 7.11 (m, 3H), 7.03 (t, J = 7.8 Hz, 1H), 6.91 (d, J = 8.2 Hz, 2H), 4.27 (s, 2H, Benzylic-CH 2 ), 3.93 (s, 3H, Aryl-OCH 3 ), 3.38 (brs, 2H, NH 2 ), 2.34 (s, 3H, Aryl-CH 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 151.5, 141.9, 136.9, 134.3, 129.1, 129.0, 123.5, 120.8, 119.7, 111.3, 63.1, 55.5, 21.1. HRMS: Calc. for C 15 H 18 N 2 O [M+H] + : 243.1497, Obser. : 243.1419 5.17 N-methyl N-phenyl hydrazine (2q) was obtained as yellow liquid (112 mg, 89%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.30 7.11 (m, 2H), 6.93 (d, J = 7.7 Hz, 2H), 6.74 (t, J = 7.3 Hz, 1H), 3.62 (brs, 2H, NH 2 ), 3.03 (s, 3H, N-CH 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 152.6, 128.9, 118.5, 113.4, 44.5. HRMS: Calc. for C 7 H 10 N 2 [M+H] + : 123.0922, Obser. : 123.0929 5.18 N-ethyl-N-phenyl hydrazine (2r) was obtained as yellow liquid (118 mg, 87%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.18 (m, 2H), 6.91 (d, J = 7.2 Hz, 2H), 6.71 (m, 1H), 3.39 (q, J = 7.1 Hz, 4H (together CH 2 and broad peak of amine)), 1.10 (t, J = 7.1 Hz, 3H, CH 3 ). 13 C NMR (125 MHz, CDCl 3 ) δ 148.4, 129.1, 117.1, 112.7, 38.4, 14.8. HRMS: Calc. for C 8 H 12 N 2 [M+H] + : 137.1079, Obser. : 137.1068 5.19 N-isopropyl-N-phenyl hydrazine (2s) was obtained as yellow liquid (109 mg, 73%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.20 7.15 (m, 2H), 6.95 (d, J = 8.0 Hz, 2H), 6.70 (t, J = 7.4 Hz, 1H), 4.00 (q, J = 6.4 Hz, 1H, iso-propyl-ch), 3.17 (s, 2H, CH 2 ), 1.08 (d, J = 6.6 Hz, 6H, 2CH 3 ). 13 C 8

NMR (125 MHz, CDCl 3 ) δ 151.5, 129.0, 118.0, 113.7, 50.6, 17.6. HRMS: Calc. for C 9 H 14 N 2 [M+H] + : 151.1235, Obser.: 151.1227 5.20 N-diphenyl hydrazine (2t) was obtained as white solid (144 mg, 81%). 1 H NMR (500 MHz, CDCl 3 ). δ 7.28 (t, J = 7.8 Hz, 4H), 7.25 7.17 (m, 4H), 6.97 (t, J = 7.3 Hz, 2H), 3.77 (brs, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 149.1, 129.0, 121.9, 119.4. HRMS: Calc. for C 12 H 12 N 2 [M+H] + :185.1079, Obser.: 185.1067 5.21 N-allyl N-phenyl hydrazine (2u) was obtained as dark yellow liquid (102 mg, 69%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.17 (t, J = 8.0 Hz, 2H), 6.96 (d, J = 8.2 Hz, 2H), 6.72 (t, J = 7.3 Hz, 1H), 5.80 (m, 1H), 5.27 5.17 (m, 2H), 3.95 (d, J = 5.8 Hz, 2H, CH 2 ), 3.50 (brs, 2H, NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 151.3, 132.6, 128.9, 118.6, 118.5, 113.7, 58.8. HRMS: Calc. for C 9 H 12 N 2 [M+H] + : 149.1079, Obser. : 148.1068 5.22 N-propargyl-N-phenyl hydrazine (2v) was obtained as brown liquid (103 mg, 71%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.28 (m, 2H), 7.08 (d, J = 8.0 Hz, 2H), 6.88 (t, J = 7.3 Hz, 1H), 4.18 (d, J = 2.3 Hz, 2H, propargyl-ch 2 ), 3.77 (brs, 2H, NH 2 ), 2.18 (t, J = 2.3 Hz, 1H, propargyl-ch) 13 C NMR (125 MHz, CDCl 3 ) δ 150.5, 128.9, 120.0, 115.1, 78.0, 73.2, 46.0. HRMS: Calc. for C 9 H 10 N 2 [M+H] + : 147.0922, Obser.: 147.0915. 9

5.23 N,N-dibenzyl hydrazine (2w) was obtained as white solid (74 mg, 33%). 1 H NMR (500 MHz, CDCl 3 ) δ 7.47 7.25 (m, 10H), 3.73 (s, 4H, Benzylic-CH 2 ), 2.81 (brs, 2H,NH 2 ). 13 C NMR (125 MHz, CDCl 3 ) δ 137.8, 129.0, 128.3, 127.2, 64.8. HRMS: Calc. for C 14 H 11 N 2 [M+H] + : 213.1392, Obser.: 213.1384. 10

6. 1 H and 13 C NMR of N,N-disubstituted hydrazines Figure 6.1 1 H and 13 C NMR of product 2a 11

Figure 6.2 1 H and 13 C NMR of product 2b 12

Figure 6.3 1 H and 13 C NMR of product 2c 13

Figure 6.4 1 H and 13 C NMR of product 2d 14

Figure 6.5 1 H and 13 C NMR of product 2e 15

Figure 6.6 1 H and 13 C NMR of product 2f 16

Figure 6.7 1 H and 13 C NMR of product 2g 17

Figure 6.8 1 H and 13 C NMR of product 2h 18

Figure 6.9 1 H and 13 C NMR of product 2i 19

Figure 6.10 1 H and 13 C NMR of product 2j 20

Figure 6.11 1 H and 13 C NMR of product 2k 21

Figure 6.12 1 H and 13 C NMR of product 2l 22

Figure 6.13 1 H and 13 C NMR of product 2m 23

Figure 6.14 1 H and 13 C NMR of product 2n 24

Figure 6.15 1 H and 13 C NMR of product 2o 25

Figure 6.16 1 H and 13 C NMR of product 2p 26

Figure 6.17 1 H and 13 C NMR of product 2q 27

Figure 6.18 1 H and 13 C NMR of product 2r 28

Figure 6.19 1 H and 13 C NMR of product 2s 29

Figure 6.20 1 H and 13 C NMR of product 2t 30

Figure 6.21 1 H and 13 C NMR of product 2u 31

Figure 6.22 1 H and 13 C NMR of product 2v 32

Figure 6.23 1 H and 13 C NMR of product 2w 33