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Reduction, of 3 ethoxy 2 cyclohexenone

Ethoxy-2-cyclohexenone is a useful intermediate in the synthesis of certain cyclohexenones. The reduction of 3-ethoxy-2-cyclohexenone with lithium aluminum hydride followed by hydrolysis and dehydration of the reduction product yields 2-cyclo-hexenone. Similarly, the reaction of 3-ethoxy-2-cyclohexenone with Grignard reagents followed by hydrolysis and dehydration of the addition product affords a variety of 3-substituted 2-cyclo-hexenones. ... [Pg.42]

Lithium aluminum hydride, in reduction of 3-ethoxy-2-cyclohexenone to 2-cyclohexenone, 40, 14 Lithium ethoxide in condensation of benzaldehyde with tripbenylcin-namylphosphonium chloride to form 1,4-diphenyl-l, 3-butadiene,... [Pg.117]

Lithium aluminum hydride in reduction of 3-ethoxy-2-cyclohexenone to... [Pg.57]

Ethanol, 2-nitro-, 41, 67 conversion to nitroethylene, 41, 71 Ether, tert-butyl phenyl, 41, 91 Etherification of cholestanol, 41, 9 with diazomethane, 41, 9 3-Ethoxy-2-cyclohexenone, 40, 41 reduction to 2-cyclohexenone, 40, 14... [Pg.57]


See other pages where Reduction, of 3 ethoxy 2 cyclohexenone is mentioned: [Pg.295]    [Pg.57]   


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