Modern Organic Synthesis an Introduction

Transcription

1 Modern Organic Synthesis an Introduction G. S. Zweifel M. H. Nantz W.H. Freeman and Company Chapter 1 Synthetic Design 1

2 What is an ideal or viable synthesis, and how does one approach a synthetic project? The overriding concern in a synthesis is the yield, including the inherent concepts of simplicity (fewest steps) and selectivity (chemoselectivity, regioselectivity, diastereoselectivity, and enantioselectivity). This chapter outlines strategies for the synthesis of target molecules based on retrosynthetic analysis. Basic Concept 1.1 Retrosynthetic Analysis The symbol signifies a reverse synthetic step and is called a transform. The main transforms are disconnections, or cleavage of C-C bonds, and functional group interconversions (FGI) Retrosynthetic analysis involves the disassembly of a TM into available starting materials by sequential disconnections and functional group interconversions(fgi). Synthons are fragments resulting from disconnection of carbon-carbon bonds of the TM. The actual substrates used for the forward synthesis are the synthetic equivalents (SE). 2

3 Synthetic design involves two distinct steps (1) Retrosynthetic analysis (2) Subsequent translation of the analysis into a forward direction synthesis. Chemical bonds can be cleaved heterolytically, homolytically, or through concerted transform. Donor and Acceptor Synthons Acceptor synthon à carbocation (electrophilic) Donor synthon à carbanion (nucleophilic) Table 1.1 Common Acceptor Synthon Synthetic equivalents 3

4 Common Acceptor Synthon Synthetic equivalents Table 1.2 Common Donor Synthons Common Donor Synthon Synthetic equivalents 4

5 Retrosynthetic Analysis A Retrosynthetic Analysis B 5

6 E-Class: Groups conferring electrophilic character to the attached carbon (+) -NH 2, -OH, -OR, =O, =NR, -X (halogens) G-Class: Groups conferring nucleophilic character to the attached carbon (-) -Li, -MgX, -AlR 2, SiR 3 A-Class: Functional Groups that exhibit ambivalent character (+ or -) -BR 2, -C=CR 2, -C CR, -NO 2, N, -SR, -S(O)R, -SO 2 R Consonant Pattern: Positive charge are placed at carbon atom bonded to the E class groups. Dissonant Pattern: One E class is bonded to a carbon with a positive charge, whereas the other E class group resides on a carbon with a negative charge. Alternating Polarity Disconnections Consonant Simple synthesis Dissonant 6

7 One Functional Group Analysis 7

8 Two Functional Groups In a 1,3-Relationship Analysis Synthesis (path b) 8

9 Two Functional Groups in 1,4-Relationship Analysis The a-carbon in this synthon requires an inversion of polarity (umpolung in German) from the negative (-) polarity normally associated with a ketone a-carbon. a-bromoketone Enolate cannot be used because of the formation of an epoxy ketone (Darzens condensation). Instead, enamine is used. Synthesis 9

10 Analysis Umpolung Synthesis 10

11 1.2 Reversal of the Carbonyl Group Polarity (Umpolung) The carbonyl group is electrophile at the carbon atom and hence is susceptible to attack by nucleophile. Reversal of polarity of a carbonyl group has been explored and systemized by Seebach. Unnatural negative charge negatively charged c carboxylic synthon Since formyl and acyl anions are not accessible, one has to use synthetic equivalents of these anions. Umpolung in a synthesis usually requires extra steps. 11

12 Formyl and Acyl anion derived from 1,3-dithianes 2-lithio-1,3dithian species; acyl anion equivalents EtSH: pka 11 (more acidic) EtOH: pka 16 12

13 With HMPA (hexamethylphosphoramide), [(Me 2 N) 3 P=O], dithiane-derived carbaions may serve as Michael donors. But without HMPA, 1,2-addition to the carbonyl group prevails. 13

14 Acylanions derived from Nitroalkanes CH 3 NO 2, pka 10.2; CH 3 CH 2 NO 2, pka 8.5 Nitronates of primary nitro compounds yield carboxylic acid. 14

15 Acyl anions derived from cyanohydrins O-protected cyanohydrins contains a masked carbonyl group with inverted polarity. 15

16 16

17 Acyl anion synthon derived from cyanohydrins may be generated catalytically by cyanide ion via the Stetter reaction. Acycl anions derived from Enol ethers 17

18 Acyl anions derived from lithium acetylide 1.3 steps in planning a synthesis Construction of the carbon skeleton Control of relative stereochemistry Functional Group interconversion Control of enantioselectivity Construction of the carbon skeleton 18

19 Important C-C bond forming reactions encountered in organic synthesis Reactions of organolithium and Grignard reagents, such as RLi, RC Cli, RMgX, and RC CMgX, with aldehyde, ketones, esters, epoxides, acid halides, and nitriles Reactions of 1 o alkyl halides with - C N to extend the carbon Alkylations of enolate ions to introduce alkyl groups to carbons adjacent to a carbonyl group (e.g., acetoacetic ester synthesis, malonic ester synthesis) Condensations such as aldol (intermolecular, intramolecular), Claisen, and Dieckmann 19

20 Michael additions, organocuprate additions (1,4-additions) Friedel-Crafts alkylation and acylation reactions of aromatic substrates Wittig reactions, and Horner-Wadsworth-Emmons olefination Diels-Alder reactions giving access to cyclohexenes and 1,4- cyclohexadienes Ring-closing olefin metathesis Table 1.3 Summary of Important Disconnections 20

21 Disconnections of bonds should be carried out only if the resultant fragments can be reconnected by known and reliable reactions. fewest number of disconnections (see Section 1.4, convergent vs. linear synthesis) It is often advantageous to disconnect at a branching point since fragments can be easily accessible, either by synthesis or from a commercial source. 21

22 A preferred disconnection of cyclic esters (lactones) or amides (lactams) produces hydroxy-carboxylic acid or aminecarboxylic acids as targets. Functional groups in the TM may be obtained by functional group interconversion. 22

23 Symmetry in the TM simplifies the overall synthesis by decreasing the number of steps required for obtaining the TM. Introduction of an activating functional group may facilitate carbon-carbon bond formation. After accomplishing its role, the activating group is removed. 23

24 The presence of a 1,6-dioxygenated compound suggests opening of a six-membered ring. A variety of cyclohexene precursors are readily available via condensation and Diels-Alder reaction or via Birch reductions of aromatic compounds. Disconnection of an internal (E)- or (Z)-double bond or a side chain of an alkene suggests a Wittig-type reaction or an alkylation of a vinylcuprate, respectively. 24

25 The presence of a six-membered ring, especially a cyclohexene derivative, suggests a Diels-Alder reaction. The structural feature of an a,b-unsaturated ketone or a b-hydroxy ketone in a six-membered ring suggests double disconnection coupled with functional group interconversions. (Robinson annulation) Functional Group Interconversion a. Alkyl Chlorides b. Alkyl Bromides 25

26 c. Allylic and Propargylic Bromides d. Alkyl Iodies e. Nitriles 26

27 f. 1 o and 2 o Alcohols g. 1 o, 2 o and 3 o Amines 27

28 h. Aldehydes and Ketones 28

29 i. Carboxylic Acids 29

30 j. Alkenes k. Alkynes 30

31 Control of Relative Stereochemistry (stereoselctive and stereospecific) S N 2 displacement reaction; E2 elimination reactions Catalytic hydrogenation of alkyne (cis product) Metal ammonia reduction of alkyne (trans product) Oxidation of alkenes with osmium tetroxide Addition of halogens, interhalogens (e.g., BrI) or halogen-like species (e.g., PhSCl, BrOH) to double bond Hydroboration reactions Epoxidation of alkenes; ring-opening of epoxide Cyclopropanation Control of enantioselectivity 31

32 1.4 Choice of Synthetic Methods The choice of a method for synthesizing a compound derived from a retrosynthetic analysis should be based on the following criteria Regiochemistry, the preferential addition of the reagent in only one of two possible regions or directions. Chemoselectivity, selective reaction of one functional group in the presence of other functional groups Stereoselectivity, the exclusive or predominant formation of one of several possible stereoisomeric products. Efficiency, fewest number of steps High yields in each step Availability and costs of starting material Most environmentally friendly route. Ideally the atoms of substrate and any additional reagents used for the reaction should appear in the final product, called atom economy 32

33 Simplicity of selected procedure. Isolation and purification of reaction products. Ability and utility to separate and recover the reaction product from other materials Possibility of a convergent synthesis or a one-pot process. Linear and Convergent Syntheses In a linear synthetic scheme, the hypothetical TM is assembled in a stepwise manner. If 80% yield is obtained in each step, 21% (0.8 7 x 100) overall yield of product can be isolated after 7 steps. If 70%, only 8% overall yield. 33

34 Convergent synthesis should be considered in which two or more fragments of the TM are prepared separately and then joined at the latest-possible stage of the synthesis. Only three stages are involved in the convergent strategy, with overall yield of 51% (0.8 3 x 100). Another important consideration in choosing a convergent protocol is that failure of a single step in a multistep synthesis does not nulify the chosen synthetic approach as whole, whereas failure of a single step in a linear scheme may require a revision of the whole plan. 34

35 Convergent syntheses involve consecutive reactions, where the reagents or catalysts are added sequently into one pot. 35

36 1.5 Domino Reactions (also called cascade or Tandem reactions) Domino-type reactions involve careful design of a multistep reaction in a one-pot sequence in which the first step creates the functionality to trigger the second reaction and so on. Robinson annulation (a Michael reaction followed by aldol condensation and dehydration) 36