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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877192Generated: October 29, 2026

(1R,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexyl(2S)-cyclopentyl(4-methylphenyl)ethanoate → (2S)-Cyclopentyl-(4-methylphenyl)acetic acid

https://huagongshe.com/reaction/877192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexyl(2S)-cyclopentyl(4-methylphenyl)ethanoateHCID 58136656—
SolventTrifluoroacetic acidHCID 6422—
Product(2S)-Cyclopentyl-(4-methylphenyl)acetic acidHCID 28293121—

Reaction Steps

50.0 g (0.140 mol) of (1R,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexyl(2S)-cyclopentyl(4-methylphenyl)ethanoate were stirred under reflux for 16 h in 500 ml of trifluoroacetic acid. The trifluoroacetic acid was then removed on a rotary evaporator and the residue was taken up in 500 ml each of water and ethyl acetate. After extraction, the organic phase was washed with saturated sodium chloride solution, dried over sodium sulfate and concentrated. The residue was taken up in 1.5 liters of water, adjusted to pH 10 with aqueous sodium hydroxide solution and washed twice with in each case 300 ml of tert-butyl methyl ether. The aqueous phase was then adjusted to pH 4 using concentrated hydrochloric acid and extracted twice with in each case 300 ml of ethyl acetate. The combined ethyl acetate extracts were dried over sodium sulfate, filtered and concentrated on a rotary evaporator. This gave 27.4 g (89% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987256B2
Source datasetuspto-grants-2015_03
ORD IDord-16c652c82ba24634a0363ca071b37075
Source noteuspto-grants-2015_03