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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590894Generated: October 26, 2026

Chlorocyclohexane → Tricyclohexylbenzene

https://huagongshe.com/reaction/590894

Reaction equation

Participants

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

Reaction Conditions

Temperature3 °C

Reaction Steps

First, 6.83 g of aluminum chloride was added to 20.0 g of benzene, and agitated while cooling at 3° C. Then, 40.4 g of cyclohexyl chloride was slowly dropped thereinto. After the completion of the dropping, the mixture was agitated at room temperature for five hours and poured into ice water. The organic phase was extracted with ethyl acetate, and the obtained organic phase was subjected to vacuum distillation at 40° C. Further, vacuum distillation was performed at 170° C., and the product was cooled to room temperature. Thereafter, 50 ml of acetone was placed thereinto, and recrystallization was carried out. The resultant crystal was collected by filtration. Thus, 14 g of tricyclohexylbenzene was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09235116B2
Source datasetuspto-grants-2016_01
ORD IDord-f89bd6f5c9d24abb8d5381c2aa50dcee
Source noteuspto-grants-2016_01