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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015377Generated: October 27, 2026

4-(4-Chlorophenyl)cyclohexane-1-carboxylic acid → [Trans-4-(4-chlorophenyl)cyclohexyl]methanol

https://huagongshe.com/reaction/1015377

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenyl)cyclohexane-1-carboxylic acidHCID 2735792—
SolventWaterHCID 962—
Product[Trans-4-(4-chlorophenyl)cyclohexyl]methanolHCID 5392585364%

Reaction Steps

4-(4-Chlorophenyl)cyclohexane carboxylic acid (0.35 g, 1.5 mmol) was reacted via Method E over 72 hours. The solid was poured into a water (40 mL) solution and extracted with ethyl acetate (EtOAc) (4×10 mL). The combined organic layers were washed with brine (40 mL) and dried over anhydrous Na2SO4. The organic layer was concentrated in vacuo to obtain [4-(4-chlorophenyl)cyclohexyl]methanol (0.210 g, 64% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985755B2
Source datasetuspto-grants-2011_07
ORD IDord-d161dfce120c4e5d8e678822da9c3586
Source noteuspto-grants-2011_07