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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703622Generated: October 30, 2026

Acetic Acid → 4-(2,4-Dihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-one

https://huagongshe.com/reaction/703622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-[4-(t-Butyldimethylsilyl)oxy-1,2-epoxy-2,6,6-trimethylcyclohexyl]but-3-en-2-oneHCID 54389374—
CatalystZincHCID 23994—
SolventChloroformHCID 6212—
Product4-(2,4-Dihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-oneHCID 5709022860.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

To 50 ml of a glacial acetic acid solution containing 600 mg of 4-[4-(t-butyldimethylsilyl)oxy-1,2-epoxy-2,6,6-trimethylcyclohexyl]but-3-en-2-one was added 8.9 g of a zinc powder at room temperature, and the mixture was vigorously stirred for 5 hours while maintaining the reaction temperature at about 40° C. To the reaction mixture was added 120 ml of chloroform, followed by stirring vigorously. Any insoluble matter was separated by filtration, and the filtrate was washed successively with water, a 5% aqueous solution of sodium hydrogen carbonate and water. The organic layer was dried over anhydrous magnesium sulfate, and the solvent, etc. were removed by distillation under reduced pressure. Purification of the resiude by silica gel chromatography gave 241 mg (yield: 55%) of 4-(2,4-dihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983723
Source datasetuspto-grants-1991_01
ORD IDord-aa2c4fb4eb26436f8ac9321b9ff4fcde
Source noteuspto-grants-1991_01