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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035324Generated: November 1, 2026

Chlorocyclohexane → Tricyclohexylbenzene

https://huagongshe.com/reaction/2035324

Reaction equation

Participants

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

Reaction Conditions

Temperature3 °C

Reaction Steps

Aluminum chloride (6.38 g) was added to 20.0 g of benzene, followed by stirring under cooling at 3° C., and 40.4 g of cyclohexyl chloride was slowly added dropwise thereto. After the dropwise addition, the resultant was stirred at room temperature for 5 hours, and the obtained reaction solution was added to ice water. The organic layer was extracted by using ethyl acetate, and the obtained organic layer was removed by distillation at 40° C. under reduced pressure. The resultant was further removed by distillation at 170° C. under reduced pressure and then cooled to room temperature, and 50 ml of acetone was added thereto to cause recrystallization. The precipitated crystals were collected through filtering, thereby obtaining 14 g of tricyclohexylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08574814B2
Source datasetuspto-grants-2013_11
ORD IDord-21951efda33b4875984a232e3799e524
Source noteuspto-grants-2013_11