Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185987Generated: October 25, 2026

Chlorocyclohexane → Tricyclohexylbenzene

https://huagongshe.com/reaction/1185987

Reaction equation

Participants

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

Reaction Conditions

Temperature3 °C

Reaction Steps

To 20.0 g of benzene, 6.83 g of aluminum chloride was added, cooled by 3° C. and stirred, and 40.4 g of cyclohexyl chloride was slowly added dropwise. After the dropwise addition, the mixture was stirred for 5 hours at room temperature and was poured into ice water. An organic phase was extracted using ethyl acetate and the obtained organic phase was distilled off at reduced pressure at 40° C. After further distilling off at reduced pressure at 170° C., the organic phase was cooled to room temperature, 50 ml of acetone was introduced and recrystallized. The precipitated crystals were filtered off and 14 g of tricyclohexylbenzene was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673538B2
Source datasetuspto-grants-2014_03
ORD IDord-15212c28defa4df88e6588c79f58b0b5
Source noteuspto-grants-2014_03