Chemistry 125: Lecture 67 April 12, 2010 Oxidizing/Reducing Alcohols Grignard Reactions Green Chemistry This For copyright notice see final page of this file Alcohol Oxidation (sec. 16.14) Stopping at Aldehyde (p. 805-6) Pyridinium Chlorochromate (Cl-CrO2O-) no water; no diol; no overoxidation (Loudon) “In practice the chromium byproduct deposits with pyridine as a sticky black tar, which can complicate matters.” (Wikipedia) Vicinal Diol Cleavage by IO4- (sec. 16.14b) Good Practice to Fill in Reagents 0:49-11:35 Alcohol (retro)Synthesis (secs. 16.13, 16.15) Hydride Reduction (sec. 16.13 p. 802) “Versatility” of Grignard Reagent (1 step from CH3OH) O from CH OH) nucleophilic(3 steps 3 carbon? CH2from O alkene O CH O O C C or Is there a preferred order? R-OH PBr3 R-Br Mg R-MgBr “Versatility” of Grignard Reagent 1) CH3MgBr O 2) H+ / H2O Cf. 2 t-Bu t-Bu-H avoid steric + hindrance CH3 O + H MgBr MgBr OH 95% H- reduction 1) t-BuMgBr t-Bu OH 2) H+ / H2O OH H H O 0% H O no H 1) t-BuCH2MgBr 2) H+ / H2O 65% CH2-t-Bu OH 35% H-CH2-t-Bu H+ + enolate ketone :-( 4% H-t-Bu + ketone 90% from Roberts & Caserio (1965) “Versatility” of Grignard Reagent H and steric hindrance Risk of Reduction from Roberts & Caserio (1965) Wittig Reaction (sec. 16.17) Ph3P is good at taking up O to form strong Ph3P=O bond. Biological Oxidation NAD+ , NADH revisited (sec. 16.18) Pharmaceuticals generate < 0.2% of the chemical industry’s product mass, but some 25% of its $ value, and >50% of its chemical waste. “Key green chemistry research areas - a perspective from pharmaceutical manufacturers” Green Chemistry, 2007, 9, 411-420 Table 1 Reactions companies use now but would strongly prefer better reagents Research Area Number of roundtable companies voting for this research area as a priority area Amide formation avoiding poor atom economy reagents 6 votes OH activation for nucleophilic substitution 5 votes Reduction of amides without hydride reagents 4 votes “Lithium aluminummethods hydride, having molecular weight of 38 and four Oxidation/Epoxidation without theause of chlorinated solvents 4 votes hydrides per molecule, has the highest hydride density and is frequently Saferused, and“…the more friendly Mitsunobu reactions 3 votes use ofit stoichiometric high-valent metals evenenvironmentally though cogenerates an inorganic by-product which is Os, virtually been eliminated difficult (Mn, toreaction separate fromhave the product…slow filtration and product loss Friedel-Crafts on Cr) unactivated systems 2 votes throughfrom occclusion or adsorptionprocesses…” are typical problems…” pharmaceutical Nitrations 2 votes End of Lecture 67 April 12, 2010 Copyright © J. M. McBride 2010. Some rights reserved. Except for cited third-party materials, and those used by visiting speakers, all content is licensed under a Creative Commons License (Attribution-NonCommercial-ShareAlike 3.0). Use of this content constitutes your acceptance of the noted license and the terms and conditions of use. Materials from Wikimedia Commons are denoted by the symbol . Third party materials may be subject to additional intellectual property notices, information, or restrictions. The following attribution may be used when reusing material that is not identified as third-party content: J. M. McBride, Chem 125. License: Creative Commons BY-NC-SA 3.0