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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018804Generated: October 31, 2026

Chlorine → 1-[3-Chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanone

https://huagongshe.com/reaction/1018804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorineHCID 24526—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-[4-(3,3,5,5-Tetramethylcyclohexyl)phenyl]ethanoneHCID 22390428—
SolventDichloromethaneHCID 6344—
Product1-[3-Chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanoneHCID 2239042574%

Reaction Conditions

Temperature0 °C

Reaction Steps

40.25 g of aluminium chloride are added at 0° C., under an inert atmosphere, to 350 ml of dichloromethane, followed by addition of 5 g of 1-[4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanone (compound V.1) dissolved in dichloromethane. After stirring for 2 hours at 0° C., 17.1 ml of chlorine gas (d=1.565, measured in the liquid state at −78° C.) are bubbled into the reaction. After warming to room temperature, a water/ice mixture is added to the reaction mixture. The resulting mixture is extracted with dichloromethane, the phases are separated after settling has taken place, and the organic phase is dried over magnesium sulphate and concentrated under reduced pressure. The residue is purified on a column of silica gel, eluting with a 7/3 (v/v) cyclohexane/dichloromethane mixutre; yield=74%; m.p.=64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482986B1
Source datasetuspto-grants-2002_11
ORD IDord-8d60e7d78c004558bd93730df4572b87
Source noteuspto-grants-2002_11