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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427410Generated: October 26, 2026

Hydrochloric Acid → 4-Phenyl-cyclohexanecarboxylic acid

https://huagongshe.com/reaction/427410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Cyclohexene-1-carboxylic acidHCID 69470—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
Product4-Phenyl-cyclohexanecarboxylic acidHCID 34481276.5%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a mixture of AlCl3 (13 g, 97.5 mmol, 1.0 equiv) in benzene (100 mL) kept at 35° C., was added 1-cyclohexenecarboxylic acid (5 g, 39.7 mmol, 0.41 equiv) dropwise. After addition was complete, the reaction solution was heated to 70° C. for 1 h and 45° C. overnight. The reaction was cooled, and 200 mL of 1 N HCl was slowly added. The product was extracted with EtOAc. The organic layer was extracted with 1 N NaOH and the aqueous layer was acidified with concentrated HCl to produce a white precipitate that was collected by filtration, washed with water and dried to give the titled compound as a white solid (3.1 g, 38%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313117B1
Source datasetuspto-grants-2001_11
ORD IDord-9304d89c4e324764996841c307a765a8
Source noteuspto-grants-2001_11