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1 C-C Bond formation Chapter 26. 2 Carbon–Carbon Bond Forming Reactions To form the carbon skeletons of complex molecules, organic chemists need an extensive.

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Presentation on theme: "1 C-C Bond formation Chapter 26. 2 Carbon–Carbon Bond Forming Reactions To form the carbon skeletons of complex molecules, organic chemists need an extensive."— Presentation transcript:

1 1 C-C Bond formation Chapter 26

2 2 Carbon–Carbon Bond Forming Reactions To form the carbon skeletons of complex molecules, organic chemists need an extensive repertoire of carbon–carbon bond forming reactions. We have earlier looked at reactions of organometallic reagents such as Grignard, organolithium and organocuprate reagents with carbonyl and other substrates to form larger molecules. The focus of this chapter will be on additional carbon–carbon bond forming reactions which utilize a variety of starting materials and conceptually different reactions. Three such reactions involve coupling of an organic halide with an organometallic reagent or alkene: (1) Organocuprate coupling reactions, (2) Suzuki reaction, and (3) Heck reaction.

3 3

4 4

5 5

6 6 Also enolates

7 7 Also enamines

8 8 Preparing organolithium reagents: Metal halogen exchange

9 9 Troublesome side reactions: Alkylation with alkylbromides from organolithium preparation Elimination reactions with alkylbromides from organolithium preparation or intended alkyl halide

10 10

11 11 Organolithium pKa’s

12 12

13 13 Organocuprate reagents react with a variety of functional groups including acid chlorides, epoxides and ,  - unsaturated carbonyl compounds. Organocuprate reagents also react with organic halides R ′ –X to form coupling products R–R′ that contain a new C–C bond. Only one R group of the organocuprate is transferred to form the product, while the other becomes part of the RCu, a reaction product. Coupling Reactions of Organocuprates

14 14 Methyl, 1 °, cyclic 2 °, vinyl, and aryl halides can be used. Reactions with vinyl halides are stereospecific. The halogen (X) may be Cl, Br, or I. Tertiary (3 ° ) halides are too sterically hindered to react. General Features of Organocuprate Coupling Reactions

15 15 Making vinyl halides for cuprate reactions

16 16 Since organocuprate reagents are prepared in two steps from alkyl halides (RX), this method ultimately converts two organic halides (RX and R ′ X) into a hydrocarbon R–R ′ with a new carbon–carbon bond. This means that using this methodology, a given hydrocarbon can often be made by two different routes. Coupling to Form Hydrocarbons

17 Retro Synthetic analysis (Cuprates) “….the grand thing is to be able to reason backwards. That is a very useful accomplishment, and a very easy one, but people do not practice it much.” Sherlock Holmes in “A Study in Scarlet” Break into equal size fragments at branch points or appropriately adjacent to functionality

18 Retro Synthetic analysis (Cuprates)

19 19 Organopalladium Mediated Reactions Suzuki Reaction Heck Reaction

20 20 During a reaction, Pd is coordinated to a variety of groups called ligands, which donate electron density to (or sometimes withdraw electron density from) the metal. A common electron donating ligand is phosphine, some derivatives of which are shown: Organopalladium Compounds

21 21 Organopalladium compounds are generally prepared in situ during the course of a reaction, from another palladium reagent such as Pd(OAc) 2 or Pd(PPh 3 ) 4. “Ac” is the abbreviation for the acetyl group, CH 3 C=O, so OAc is the abbreviation for CH 3 CO 2 −. In most useful reactions, only a catalytic amount of Pd reagent is used. Two common processes, called oxidative addition and reductive elimination, dominate many reactions of palladium compounds. Organopalladium Compounds

22 22 Oxidative Addition and Reductive Elimination

23 23 The Suzuki reaction is a palladium-catalyzed coupling of an organic halide (R ′ X) with an organoborane (RBY 2 ) to form a product (R–R ′ ) with a new C–C bond. Pd(PPh 3 ) 4 is the typical palladium catalyst. The reaction is carried out in the presence of a base such as NaOH or NaOCH 2 CH 3. Vinyl or aryl halides are most often used, and the halogen is usually Br or I. The Suzuki reaction is completely stereospecific. Details of the Suzuki Reaction

24 24 Examples of the Suzuki Reaction

25 25 Two types of organoboranes can be used in the Suzuki reaction: vinylboranes and arylboranes. Vinylboranes, which have a boron atom bonded to a carbon– carbon double bond, are prepared by hydroboration using catecholborane, a commercially available reagent. Hydroboration adds H and B in a syn fashion to form a trans vinylborane. With terminal alkynes, hydroboration always places the boron atom on the less substituted terminal carbon. Organoboranes in Suzuki Reaction

26 26 Arylboranes, which have a boron atom bonded to a benzene ring, are prepared from organolithium reagents by reaction with trimethyl borate [B(OCH 3 ) 3 ]. Preparation of Arylboranes

27 27

28 28 Synthesis Using the Suzuki Reaction The Suzuki reaction was a key step in the synthesis of bombykol, the sex pheromone of the female silkworm moth. The synthesis of humulene illustrates that an intramolecular Suzuki reaction can form a ring. Figure 26.2

29 29 Retrosynthetic Analysis of Suzuki Reaction Aryl-Aryl links Aryl-Alkenyl links Alkenyl-Alkenyl links

30 30 Synthesis using Suzuki Coupling reaction in Loy Lab New monomers for making flame resistant polymers

31 31 The Heck reaction is a Pd-catalyzed coupling of a vinyl or aryl halide with an alkene to form a more highly substituted alkene with a new C–C bond. One H atom of the alkene starting material is replaced by the R’ group of the vinyl or aryl halide. Palladium(II) acetate [Pd(OAc) 2 ] in the presence of a triarylphosphine [P(o-tolyl) 3 ] is the typical catalyst. The reaction is carried out in the presence of a base such as triethylamine. The Heck Reaction

32 32 The alkene component is typically ethylene or a monosubstituted alkene (CH 2 =CHZ). The halogen is typically Br or I. When Z=Ph, COOR or CN in a monosubstituted alkene, the new C – C bond is formed on the less substituted carbon to afford a trans alkene. When a vinyl halide is used as the organic halide, the reaction is stereospecific. The Heck Reaction

33 33 Examples of the Heck Reaction

34 34 To use the Heck reaction in synthesis, you must determine what alkene and what organic halide are needed to prepare a given compound. To work backwards, locate the double bond with the aryl, COOR, or CN substituent, and break the molecule into two components at the end of the C=C not bonded to one of these substituents. Using the Heck Reaction in Synthesis

35 35

36 36 Retrosynthetic Analysis of Heck Reaction Advantage over Suzuki Coupling: fewer steps (No boranic ester is needed)

37 37 Heck Reaction in Loy Lab Dye for making fluorescent nanoparticles

38 38 A carbene, R 2 C:, is a neutral reactive intermediate that contains a divalent carbon surrounded by six electrons—the lone pair, and two each from the two R groups. These three groups make the carbene carbon sp 2 hybridized, with a vacant p orbital extending above and below the plane containing the C and the two R groups. The lone pair occupies an sp 2 hybrid orbital. Carbenes Singlet carbene

39 39 Dihalocarbenes, :CX 2, are especially useful reactive intermediates since they are readily prepared from trihalomethanes (CHX 3 ) by reaction with strong base. For example, treatment of chloroform (CHCl 3 ) with KOC(CH 3 ) 3 forms dichlorocarbene, :CCl 2. Dichlorocarbene is formed by a two-step process that results in the elimination of the elements of H and Cl from the same carbon. Loss of the two elements from the same carbon is called  elimination. Dihalocarbenes

40 40

41 41 Since dihalocarbenes are electrophiles, they readily react with double bonds to afford cyclopropanes, forming two new carbon–carbon bonds. Dihalocarbenes in Cyclopropane Synthesis

42 42 Cyclopropanation is a concerted reaction, so both bonds are formed in a single step. Carbene addition occurs in a syn fashion from either side of the planer double bond. Carbene addition is a stereospecific reaction, since cis and trans alkenes yield different stereoisomers as products. Carbene Addition to Alkenes

43 43 Methylene, The Simplest Carbene Methylene, :CH 2, is readily prepared by heating diazomethane, which decomposes and loses nitrogen. The reaction of methylene produced in this manner with an alkene often leads to a complex mixture of products. Thus the reaction cannot be reliably used for cylcopropane synthesis.

44 44 Polymerization of carbenes: Thermal of Lewis acid catalyzed Noble metal catalyzed

45 45 Polymerization of carbenes: Mechanism Carbene insertions

46 46 Nonhalogenated cyclopropanes can be prepared by the reaction of an alkene with diiodomethane, CH 2 I 2, in the presence of a copper-activated zinc reagent called zinc– copper couple [Zn(Cu)]. This is known as the Simmons–Smith reaction. The reaction is stereospecific. The Simmons–Smith Reaction

47 47

48 48 Alkene (olefin) metathesis is a reaction between two alkene molecules that results in the interchange of the carbons of their double bonds. Two  and two  bonds are broken and two new  and two new  bonds are formed. Alkene Metathesis

49 49 Olefin metathesis occurs in the presence of a complex transition metal catalyst that contains a carbon–metal double bond. The metal is typically ruthenium (Ru), tungsten (W), or molybdenum (Mo). In a widely used catalyst called Grubbs catalyst, the metal is Ru. Metathesis catalysts are compatible with the presence of many functional groups (such as OH, OR, and C=O). Catalysts for Metathesis

50 50 Because olefin metathesis is an equilibrium process and with many alkene substrates yields a mixture of starting material and two or more alkene products, it is useless for preparative processes. However, with terminal alkenes, one metathesis product is ethylene gas (CH 2 =CH 2 ), which escapes from the reaction mixture and drives the equilibrium to the right. Thus, monosubstituted alkenes (RCH=CH 2 ) and 2,2- disubstituted alkenes (R 2 C=CH 2 ) are excellent metathesis substrates because high yields of a single alkene product are obtained. Usefulness of Metathesis Reactions

51 51 Examples of Alkene Metathesis

52 52 Figure 26.2 Drawing the Products of Alkene Metathesis

53 53

54 54 Retrosynthetic Analysis of Metathesis Reaction Are precursors available? Will cross reaction ( R ≠ R’) be dominant

55 55 ? ?

56 56 Metathesis in Loy Lab

57 57 When a diene is used as a starting material, ring closure occurs. These reactions are typically run in very dilute solution so that the reactive ends of the same molecule have a higher probability of finding each other. High dilution favors intramolecular rather than intermolecular metathesis. Ring Closing Metathesis (RCM)

58 58 Ring Closing Metathesis (RCM) in Synthesis Epothilone A is a promising anticancer agent that was first isolated from soil bacteria from the banks of the Zambezi River in South Africa. Sch38516 is an antiviral agent active against influenza A.

59 59 Ring Opening Metathesis Polymerization Poly(norbornene)

60 60 Ring Opening Metathesis Polymerization Of benzvalene Benzvalene is a less stable isomer of benzene ΔH = -282 kJ/mole

61 61 General synthesis strategies 1)Build carbon framework with enolate reactions and other C-C bond building reactions (Suzuki, Heck, Metathesis, Cuprates, Diels-Alder, & more.) 1)Use functionalities to activate C-C bond building chemistry 2)Functional group conversions to provide desired organic substituents

62 62 Directions in Synthesis 1)Regio- and stereochemical specificity 1)More atom efficiency (less waste). 1)Reactions using aqueous or non-toxic solvents (H 2 O, alcohols) 2)Reactions using less hazardous starting materials

63 63 Some practice: How would you make 1,7-diphenylheptane

64 64 Some practice: How would you make (Z)-cyclooctene

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