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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265446Generated: November 1, 2026

Potassium Hydroxide → 2-(3-Chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acid

https://huagongshe.com/reaction/1265446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-(3-Chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acid methyl esterHCID 12067652—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(3-Chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acidHCID 1206765389.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(3-chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acid methyl ester (4.85 g, 15.50 mol) in ethanol (108 mL) was treated with a solution of potassium hydroxide (4.35 g, 77.50 mmol) in water (25.2 mL). The reaction mixture was stirred at 25° C. for 3 h. The reaction mixture was then concentrated in vacuo to remove ethanol. The resulting aqueous residue was acidified to pH=2 with a 1N aqueous hydrochloric acid solution and then extracted with methylene chloride (3×15 mL). The combined organic layers were then dried over sodium sulfate, filtered, and concentrated in vacuo to afford 2-(3-chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acid (4.14 g, 89.4%) as a white solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545155B2
Source datasetuspto-grants-2003_04
ORD IDord-5f6a4d3888be48e992d53df3c6262618
Source noteuspto-grants-2003_04