1. Synthesis Making molecules you want from the ones you have.

2. Synthesis Requires Two Things a. a library of reactions b. a strategy or plan for combining known reactions to reach the desired target molecule c. and a little luck always helps

3. A library of reactions Functional group manipulations Oxidations, reductions, substitutions etc. Carbon-carbon bond formations Used to build the carbon skeleton of the target molecule

4. How does a carbocation react? Since the carbocation is a Lewis acid It can react with a Lewis base. The electron pair on the base attacks the electron deficient center

5. How else can a carbocation gain stability? Instead of reacting as a Lewis acid it can react as a Bronstead acid and donate a proton!

6. This is called an elimination reaction Because H + is eliminated from the molecule

7. Addition Elimination

8. Elimination often competes with substitution. Just like substitution where there are two forms S N 1 and S N 2 there are two forms of elimination, E1 and E2. Sorting it all out is pretty complicated, something we are not going to do.

9. But we would like to use elimination as a synthetic reaction. So how can you favor elimination? Use a very strong base that is a poor nucleophile. For example potassium t-butoxide.

10. potassium t-butoxide very strong base but steric bulk prevents t-butoxide from readily forming ethers in a substitution reaction

12. The alkene with the most substituents is the most stable and the most favored product.

14. Similar eliminations can take place with alcohols. Catalyzed by concentrated strong acids Concentrated acids are hydrophilic and will remove water from other molecules in order to dilute themselves.

15. But you can get complicated mixtures.

16. Alkyne synthesis Elimination of two moles of HBr from neighboring carbon atoms will give an alkyne.

18. You can reduce alkynes back to alkenes

19. Hydrogens come in from the same side.

20. You can reduce alkynes back to alkenes

21. For the trans isomer use a different reducing agent. Sodium metal in ammonia. Complicated mechanism.

22. pKa values

23. Sodium amide is a very strong base It can be used to form an acetylide

24. Acetylides will give us our first carbon-carbon bond making reaction. Acetylides are strong bases and good nucleophiles. They can undergo substitution reactions with primary alkyl halides.

27. Two ways to make many acetylenes

28. Now that we have a carbon-carbon bond forming reaction we are ready for some real synthesis. Suppose you wanted to synthesize 3-hexanol But your only carbon containing starting materials are compounds with four carbons or less.

29. Analyze carbon framework first. Which carbon-carbon bonds must be put together in our synthesis? We could make the bond between carbons 3 and 4. But we will chose to make the new C-C bond between carbons 2 and 3.

30. No regiochemistry control Work backwards

33. One simple reaction you did in the lab. Ester Synthesis

34. Much faster

36. Butyl butyrate odor of pineapples How could you make it from 1-butanol?

38. The last reaction we are going to study. The Grignard Reaction Reaction of an nucleophilic carbon atom with a carbonyl group.

39. The Grignard Reaction

41. The Grignard Reaction converts aldehydes or ketones to alcohols.

44. Reactions with aldehydes give secondary alcohols

45. 2. H +

46. Pheromone of the European Bark Beetle How could you synthesize it from organic compounds with four carbons or less? First analyze the carbon skeleton Then work backwards.

49. or

51. Odor of Rum

52. Syntheses of Discodermolides Useful for Investigating Microtubule Binding and Stabilization Deborah T. Hung, Jennie B. Nerenberg, and Stuart L. Schreiber* Contribution from the Howard Hughes Medical Institute, Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138 J. Am. Chem. Soc. 1996, 118, 11054 - 11080 CHE 503 Organic Synthesis Professor Frank Fowler

53. Isolated from a marine sponge

54. For geometric isomers are possible. Only one is the correct compound.

55. Isolated from a marine sponge

56. How Many Stereoisomers? = isomer choice 2 16 = 65,536 isomers

58. Possible Grignard? No, too reactive, use some acetylene chemistry instead.

60. Isolated from a marine sponge