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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071917Generated: November 3, 2026

Acetic Acid → 1-[4-(3,3,5,5-Tetramethylcyclohexyl)phenyl]ethanone

https://huagongshe.com/reaction/1071917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1-[4-(Hydroxy-3,3,5,5-tetramethylcyclohexyl)phenyl]ethanoneHCID 22390420—
CatalystZincHCID 23994—
SolventAcetonitrileHCID 6342—
Product1-[4-(3,3,5,5-Tetramethylcyclohexyl)phenyl]ethanoneHCID 2239042868%

Reaction Steps

38.1 ml of chlorotrimethylsilane are added over 45 minutes to a solution of 40.45 g of 1-[4-(hydroxy-3,3,5,5-tetramethylcyclohexyl)phenyl]ethanone (compound V′.1) and 56.21 g of sodium iodide in 230 ml of anhydrous acetonitrile. During the addition, the temperature is maintained between 35° C. and 40° C. After stirring for 2 hours, 40 ml of acetonitrile and 39.4 ml of acetic acid are added. Next, 29.4 g of finely powdered zinc are added portionwise with stirring and at room temperature. The reaction mixture is refluxed with vigorous stirring for 4 hours. After cooling to room temperature, the reaction medium is filtered through Celite and then washed with saturated aqueous sodium bicarbonate solution. The organic phase is concentrated under reduced pressure and the oil obtained is purified by chromatography on a column of silica gel, eluting with a 95/5 (v/v) cyclohexane/ethyl acetate mixture; yield=68% ; m.p.=54° C. The following compounds are obtained in the same way:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908914B1
Source datasetuspto-grants-2005_06
ORD IDord-bcc95865f78244be8ee353f2f4406c36
Source noteuspto-grants-2005_06