1 / 18

Chapter 16: Ethers, Epoxides, and Sulfides 16.1: Nomenclature of Ethers, Epoxides, and Sulfides

Chapter 16: Ethers, Epoxides, and Sulfides 16.1: Nomenclature of Ethers, Epoxides, and Sulfides (Please read) 16.2: Structure and Bonding in Ethers and Epoxides The ether oxygen is sp 3 -hybridized and tetrahedral. In general, the C-O bonds of ethers have low reactivity.

preginald
Download Presentation

Chapter 16: Ethers, Epoxides, and Sulfides 16.1: Nomenclature of Ethers, Epoxides, and Sulfides

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Chapter 16: Ethers, Epoxides, and Sulfides 16.1: Nomenclature of Ethers, Epoxides, and Sulfides (Please read) 16.2: Structure and Bonding in Ethers and Epoxides The ether oxygen is sp3-hybridized and tetrahedral. In general, the C-O bonds of ethers have low reactivity. 16.3: Physical Properties of Ethers The O-H group of alcohols act as both an H-bond donor (Lewis acid) and H-bond acceptor (Lewis base). Ethers are only H-bond acceptors (Lewis base) 16.4: Crown Ethers (Please read)

  2. 16.5: Preparation of Ethers • Acid-Catalyzed . . . • Condensation of Alcohols (not very useful) (Chapter 15.7) • Addition of Alcohols to Alkenes (recall hydration of Alkenes in chapter 6.9)

  3. 2) The Williamson Ether Synthesis (Chapter 16.6) (The workhorse of ether syntheses) Reaction of an alkoxide with an alkyl halide or tosylate to give an ether. Alkoxides are prepared by the reaction of an alcohol with a strong base such as sodium hydride (NaH) The Williamson ether synthesis is an SN2 reaction.

  4. The Williamson Ether Synthesis: • Few restrictions regarding the nature of the the alkoxide • Works best for methyl- and 1°-halides or tosylates. • E2 elimination is a competing reaction with 2° -halides or tosylates • 3° halides undergo E2 elimination • Vinyl and aryl halides do not react

  5. 16.7: Reaction of Ethers: A Review and Preview (please read) The reactivity of the ether functional group is low Over time ethers can react with O2 to form hydroperoxides 16.8: Acid-Catalyzed Cleavage of Ethers Recall the reaction of an alcohol with HX to give a halide (Ch. 4.12) RCH2-OH + H-X RCH2-X + H2O The mechanism for the acid clevage of ethers is similar RCH2-O-R’ + H-X RCH2-X + HO-R’

  6. RCH2-O-CH2R’ + H-X RCH2-X + R’CH2-OH

  7. 16.9: Preparation of Epoxides: A Review and Preview Expoxidation of alkenes (chapter 6.19) Base promoted ring closure of a vicinal halohydrin (Chap. 6.17) (this is an intramolecular Williamson ether synthesis)

  8. 16.10: Conversion of Vicinal Halohydrins to Epoxides An Intramolecular Williamson synthesis

  9. 16.11: Reactions of Epoxides: A Review and Preview Nucleophilic epoxide ring-opening by Grignard reagents (15.4) b) Epoxide ring-opening by other nucleophiles c) Acid-catalyzed epoxide ring-opening

  10. 16.12: Nucleophilic Ring Opening of Epoxides: The ring opening of an epoxide is an SN2 reaction with nucleophiles such as amines and the anion of alcohols and thiols Reductive opening of epoxide is achieved with LiAlH4

  11. 16.13: Acid-Catalyzed Ring Opening of Epoxides: Epoxide opening with H-X gives a vicinal halohydrin

  12. Preparation of syn- and anti- vicinal diols (15.5) 16.14 Epoxides in Biological Processes (please read) In cells, epoxidation of C=C is carried out by enzymes called monooxygenases such cytochrome P450’s, flavoenzymes, etc., which activate O2 and catalyze the oxygen transfer reaction

  13. Bioactivation and detoxication of benzo[a]pyrene diol epoxide: Glutathione (G-SH)

  14. 16.15: Preparation of Sulfides Reaction of a thiolate anions with 1° and 2° alkyl halides and tosylates (analogous to the Williamson ether synthesis) R-SH + NaOH R-S- Na+ R-S-CH2R’ alcohol or water solvent R’-CH2X pKa ~ 16-18 pKa ~ 11 Thiolates are more reactive nucleophiles and less basic than alkoxides

  15. 16.16: Oxidation of Sulfides: Sulfoxides and Sulfones (please read) Unlike ethers, sulfides can be oxidized to sulfoxides and further oxidized to sulfones sulfide sulfoxide sulfone 16.17: Alkylation of Sulfides: Sulfonium Salts (Please read) The sulfur atom of sulfides is much more nucleophilic than the oxygen atom of ethers, and will react with alkyl halides to give stable sulfonium salts. See S-adenosylmethionine (p. 709)

  16. 16.18: Spectroscopic Analysis of Ethers, Epoxides and Sulfides IR spectroscopy: not particularly diagnostic for the ether functional group. Strong C-O single bond stretch between 1050-1150 cm-1 1H NMR: protons on the carbons that are part of the ether linkage are deshielded relative to alkanes. The chemical shift of these protons is from = 3.0 - 4.0 ppm 13C NMR: the chemical shift of carbons that are part of the ether linkage are in the range of = 50 - 80 ppm C-O-C H3C-H2C-H2C-O-CH2-CH2-CH3

  17. = 2.8, dd, J= 5.5, 2.6, 1H Protons and carbon resonances of an epoxide are shielded relative to those of a typical ethers 1H NMR: = 2.2 - 3.2 ppm 13C NMR: = 40 - 60 ppm = 3.6, dd, J= 4.1, 2.6 1H = 3.1, dd, J= 5.5, 4.1, 1H = 7.4-7.1, m, 5H 125.5 128.5 128.1 52.3 51.0 CDCl3 137.7

  18. C9H10O2 dd J= 4.2, 4.8 dd J= 2.6, 4.8 dd J= 3.4, 11.0 dd J= 6.0, 11.0 m 1H 1H 1H 3H 1H 1H 2H 129.54 114.64 68.68 44.76 121.25 50.18 158.49

More Related