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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306334Generated: November 1, 2026

Methanol → 3-Cyclopentyl-2-(4-fluoro-3-trifluoromethyl-phenyl)-propionic acid methyl ester

https://huagongshe.com/reaction/2306334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant3-Cyclopentyl-2-(4-fluoro-3-trifluoromethyl-phenyl)-propionic acidHCID 12069500—
Product3-Cyclopentyl-2-(4-fluoro-3-trifluoromethyl-phenyl)-propionic acid methyl esterHCID 1206950187.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3-cyclopentyl-2-(4-fluoro-3-trifluoromethyl-phenyl)-propionic acid (7.77 g, 25.3 mmol) in methanol (50 mL) was treated slowly with concentrated sulfuric acid (0.01 mL). The resulting reaction mixture was heated under reflux for 24 h. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo. The residue was dissolved in ethyl acetate (75 mL) and washed with a saturated aqueous sodium bicarbonate solution (1×50 mL), water (1×50 mL), and a saturated aqueous sodium chloride solution (4×50 mL). The combined organic layers were dried over magnesium sulfate and sodium sulfate, filtered, and concentrated in vacuo to afford 3-cyclopentyl-2-(4-fluoro-3-trifluoromethyl-phenyl)-propionic acid methyl ester (8.48 g, 87.5%) as yellow oil: EI-HRMS m/e calcd for C16H18F4O2 (M+) 318.1243, found 318.1240.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441184B1
Source datasetuspto-grants-2002_08
ORD IDord-f06a0506ec904cd596ff42262da04841
Source noteuspto-grants-2002_08