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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509373Generated: November 2, 2026

Chlorocyclohexane → Tricyclohexylbenzene

https://huagongshe.com/reaction/1509373

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 numberUS09223208B2
Source datasetuspto-grants-2015_12
ORD IDord-f5730cd145cd472990cbe52166e95ab4
Source noteuspto-grants-2015_12