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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935220Generated: October 26, 2026

Water → 2-(4-Benzyloxy-phenyl)-3-cyclopentyl-propionic acid

https://huagongshe.com/reaction/1935220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Benzyloxy-phenyl)-3-cyclopentyl-propionic acid methyl esterHCID 67483155—
SolventMethanol tetrahydrofuran waterHCID 21892291—
Product2-(4-Benzyloxy-phenyl)-3-cyclopentyl-propionic acidHCID 2246790460.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(4-benzyloxy-phenyl)-3-cyclopentyl-propionic acid methyl ester (1.38 g, 4.08 mmol) in tetrahydrofuran/water/methanol (10.2 ml, 3:1:1) was treated with a 2N aqueous sodium hydroxide solution (3.06 mL, 6.12 mmol). The reaction was stirred at 25° C. for 16 h. At this time, an additional amount of the 2N aqueous sodium hydroxide solution (3.06 mL, 6.12 mmol) was added. The reaction was stirred at 25° C. for an additional 24 h. At this time, the reaction mixture was poured into water and extracted into methylene chloride. The layers were separated. The aqueous layer was acidified to pH=1 with a 1N aqueous hydrochloric acid solution and was then extracted with a solution of methylene chloride/methano (90/10). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 50/50 hexanes/ethyl acetate) afforded 2-(4-benzyloxy-phenyl)-3-cyclopentyl-propionic acid (0.79 g, 60.2%) as a white solid: mp 112-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384220B2
Source datasetuspto-grants-2002_05
ORD IDord-1924d089a48c493f90a77158de1f36fc
Source noteuspto-grants-2002_05