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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398481Generated: October 29, 2026

Methanol → 3-Cyclopentyl-2-(4-trifluoromethylsulfanylphenyl)propionic acid methyl ester

https://huagongshe.com/reaction/398481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 22315105HCID 22315105—
CatalystSulfuric AcidHCID 1118—
Product3-Cyclopentyl-2-(4-trifluoromethylsulfanylphenyl)propionic acid methyl esterHCID 4622138399%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3-cyclopentyl-2-(4-trifluoromethylsulfanyl-phenyl)propionic acid (1.33 g, 4.18 mmol) in methanol (10 mL) was treated slowly with 4 drops of concentrated sulfuric acid. The resulting reaction mixture was heated under reflux for 36 h. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo to remove methanol. The residue was diluted with ethyl acetate (200 mL). The organic phase was washed with a saturated aqueous sodium bicarbonate solution (1×100 mL) and a saturated aqueous sodium chloride solution (1×100 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 97/3 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-trifluoromethylsulfanyl-phenyl)propionic acid methyl ester (1.37 g, 99%) as a light yellow oil: EI-HRMS m/e calcd for C16H19F3O2S (M+) 332.1058, found 332.1052.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-b5ffa660849f444ea629729e543d9a2b
Source noteuspto-grants-2003_08