Objective 14. Develop synthesis strategies for organic synthesis.

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Objective 14. Develop synthesis strategies for organic synthesis. Skills: Draw structure ID structural features and reactive sites (alpha C, beta C, LG, etc.) ID Nu - and E + use curved arrows to show bonds breaking and forming show delocalized electrons with resonance structures. Key ideas: Starting material --> target compound. Count # of C s bigger or smaller compound. ID functional groups in starting material and target compound. What part(s) of the starting material and target compound are the same? ID bonds that break/form. Brainstorm possible reactions.

Reaction Roadmap: Which groups has an α-c? (2 types of α-c) What are β-keto acids/esters used for? What group makes α,β-unsaturated carbonyls? alkyne alkane alkene alkyl halide amide acid ester alcohol R-M aldehyde ketone nitriles Diols, cyanohydrins, imines epoxide Ether acetal w/ ROH

The Journey!

ORGANIC SYNTHESIS STRATEGIES Convert one functional group to another Move a Functional Group from 1 C to adjacent C Make a C-C bond to make a bigger molecule Break a C-C bond to make a smaller molecule How? See Structural Features è Tells you Reaction Type

Structural Features tell us: Which atom or bond reacts Reaction Type How to make a Compound C=C pi bond (including conjugated diene and aromatic) C-O, C-X, C-N compounds: α carbon, leaving group (HOH, ROH, NH 3, X - ), H bonded to βcarbon, epoxide C=O compounds: carbonyl carbon, carbonyl oxygen, αcarbon (C next to carbonyl C), βcarbon TWO structural features: β-hydroxy aldehyde/ketone (see enolates) α,β-unsaturated aldehyde/ketone (see enolates) β-keto ester (see ester enolates)

Structural Features Acid H (see pk table) Base (see pk table) α carbon, LG Reacts with Nu: - Reaction Type Acid-Base Nucleophilic Substitution Product Base Acid ROH, RX, etc Carbonyl C on Acid or Acid Derivative LG Nucleophilic Acyl Substitution Acid or Acid Derivative Aromatic EAS Mono-, polysub aromatic α carbon, H bonded to βcarbon, LG Reacts with Nu: - C=C pi bond Reacts with E + Carbonyl C on RCHO, RCOR Elimination Electrophilic Addition Nucleophilic Addition C=C bond ROH, RX, etc. Acetal, imine, etc.

Many Organic Reactions are Reversible Example: OR How does ethanol react? How can you make ethanol? Ethanol Structural Features: α carbon and LG ==> Substitution H bonded to βcarbon and LG ==> Elimination Basic O and Acidic H ==> Acid-Base C-O bond ==> Oxidation Several Ways Ethanol Reacts è Several Ways to Make Ethanol

ORGANIC SYNTHESIS STRATEGIES How? See Structural Features è Tells you Reaction Type Convert One Functional Group To Another Structural Features: α carbon and LG ==> Substitution Structural Features: carbonyl C, LG ==> Substitution (acyl)

ORGANIC SYNTHESIS STRATEGIES How? See Structural Features è Tells you Reaction Type Convert One Functional Group To Another Structural Features: C-O bond to C-O, C=O ==> Oxidation

C&EN, 6/2/14, p. 24 (http://cen.acs.org/articles/92/i23/cleaning-conundrum.html ) Eastman Chemical Invents a New Cleaning Solvent for household and industrial cleaning products that meets the EPA standards for toxicity and VOC content. Trade Name: Omnia Propose an efficient synthesis of Omnia from Replaces: ethylene glycol monobutyl ether (CA hazardous substance) dipropylene glycol monomethyl ether (VOC)

ORGANIC SYNTHESIS STRATEGIES How? See Structural Features è Tells you Reaction Type Move a Functional Group from 1 C to adjacent C Structural Features: α C and LG è Sub RBr è make by Sub H on β C and LG è Elim RBr è make by Addition

ORGANIC SYNTHESIS STRATEGIES How? See Structural Features è Tells you Reaction Type Move a Functional Group from 1 C to adjacent C Structural Features: C=C pi bond è Addition C=C pi bond è make by Elim

ORGANIC SYNTHESIS STRATEGIES How? See Structural Features è Tells you Reaction Type Make a C-C bond to make a bigger molecule Use a carbon nucleophile and a carbon electrophile ID structural features: addition ID structural features: substitution Which C is electrophilic? Which carbon nucleophile to use? RMgX, CN -, acetylide ion, enolate or ester enolate

Compare C-C bond making methods: 1. Grignard (to make ROH) 2. Acetylide ion (alkyne ---> other functional groups) 3. CN substitution (to make nitrile ---> convert to acid) 4. Enolate ion (Aldol, Claisen, RX, malonic ester, acetoacetic ester)

Note: Aldol and Claisen reactions form a C-C bond What else can an enolate or ester enolate ion react with? +?? --------> +?? -------->

Propose an efficient synthesis of Omnia from Trade Name: Omnia Structural Features: carbonyl C and carbonyl O (ester) H on α C OH on β C (β-hydroxy ester, not a β-keto ester) O-H group: O is basic, H is acidic

Use Enolate in Nu: - substitution reaction Problems with this method: 1. Elimination competes with substitution 2. Poor yield Is there a Better way? (Klein, Organic Chemistry, p. 1063)

Objective: use malonic ester synthesis and acetoacetic ester synthesis to make a C-C bond α to carbonyl C Malonic ester synthesis: Lengthen chain by 2 carbons Use diethyl malonate Remove α-h to form enolate Enolate = Nu: - Acetoacetic ester synthesis: Lengthen chain by 3 carbons Use ethyl acetoacetate Remove α-h to form enolate

Alkylate the α carbon in an aldehyde/ketone: Use Acetoacetic Ester. Alkylate α carbon in an organic acid: Use Malonic Ester. Decarboxylation Reactions Are Important in Biology

Other ORGANIC SYNTHESIS STRATEGIES Shorten (Break C-C bond) a carbon chain: 1. ozonolysis 2. Decarboxylation Reaction Dicarboxylic acid (with 1 C between -COOH) -- heat --> acid + CO 2 E.g., Malonic acid (propanedioic acid) decarboxylation: Which bond breaks?

Other ORGANIC SYNTHESIS STRATEGIES Shorten (Break C-C bond) a carbon chain: 2. Break a C-C bond by decarboxylation of a. dicarboxylic acid b. β-keto acid -- heat --> CO 2 + enol ----> ketone 1 C from -COOH is α-c Draw structure of product 2 C from -COOH is β-c

Use of Acetoacetic ester and Decarboxylation in synthesis Draw the structure of each intermediate 4. heat

Other ORGANIC SYNTHESIS STRATEGIES Shorten (Break C-C bond) a carbon chain: 3. Biology: Glucose (C 6 ) undergoes glycolysis to form pyruvate (C 3 ). (10 steps. 4 th step = reverse aldol condensation breaks C-C bond) Which bond breaks?

Identify Compounds A, B, and C in the following synthetic sequence. NaOCH 2 CH 3 Compound A (C 6 H 10 O 2 ) ------------------> + H 2 C(CO 2 CH 2 CH 3 ) 2 ethanol Compound B (C 13 H 22 O 6 ) heat CH 3 CH(CH 2 CO 2 H) 2 <-------------- Compound C (C 7 H 10 O 6 ) H 2 C(CO 2 CH 2 CH 3 ) 2 = malonic ester

Conjugated dienes undergo 1,2 and 1,4 addition (Klein, Ch. 17) α,β-unsaturated ketones undergo 1,2 and 1,4 addition (Michael Reaction) How do you make an α,β -unsaturated ketone?

Common Michael Donors and Acceptors (see Klein, Table 22.2, p. 1067) Michael Donors Michael Acceptors R 2 CuLi (RMgX too strong)