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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464876Generated: October 31, 2026

Chlorocyclohexane → Tricyclohexylbenzene

https://huagongshe.com/reaction/1464876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorocyclohexaneHCID 10952—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
ProductTricyclohexylbenzeneHCID 301543350.7%

Reaction Conditions

Temperature3 °C

Reaction Steps

Aluminum chloride (6.83 g) was added to 20.0 g of benzene, and the mixture was stirred under cooling at 3° C. Thereto, 40.4 g of cyclohexyl chloride was slowly added dropwise. After the dropwise addition, the mixture was stirred at room temperature for 5 hours and then poured in ice water. The organic layer was extracted with ethyl acetate, and the obtained organic layer was distilled at 40° C. under reduced pressure, further distilled at 170° C. under reduced pressure, then cooled to room temperature, and recrystallized by charging 50 ml of acetone. The precipitated crystal was collected by filtration to obtain 14 g of tricyclohexylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999621B2
Source datasetuspto-grants-2015_04
ORD IDord-08137f861f4e4d6dae76c3d526fbcaa2
Source noteuspto-grants-2015_04