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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480253Generated: October 25, 2026

4-Phenyl-cyclohexanecarboxylic acid → (4-Phenylcyclohexyl)methanol

https://huagongshe.com/reaction/480253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenyl-cyclohexanecarboxylic acidHCID 344812—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(4-Phenylcyclohexyl)methanolHCID 3100608136%

Reaction Steps

A suspension of LiAlH4 (0.56 g, 14.8 mmol, 2.0 equiv) was prepared under argon in 50 mL of anhydrous THF (50 mL) kept at 0° C. A solution of 4-phenyl-cyclohexanecarboxylic acid (1.5 g, 7.34 mmol, 1.0 equiv) in 50 mL of THF was added dropwise over a 20 min period. The reaction mixture was stirred at ambient temperature for 1.5 h and then cooled to 0° C. The excess hydride reagent was carefully quenched under argon by dropwise addition of 1 N HCl. After quenching, the reaction mixture was extracted with EtOAc. The organic layer was dried over MgSO4, filtered and concentrated to give the title product as a colorless oil (1.9 g crude) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649642B2
Source datasetuspto-grants-2003_11
ORD IDord-56cd780c090840b79dbc6643f62ad871
Source noteuspto-grants-2003_11