Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860125Generated: November 1, 2026

Methanol → 2-(4-Bromo-phenyl)-3-cyclopentyl-propionic acid methyl ester

https://huagongshe.com/reaction/1860125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-(4-Bromo-phenyl)-3-cyclopentyl-propionic acidHCID 22315094—
CatalystSulfuric AcidHCID 1118—
Product2-(4-Bromo-phenyl)-3-cyclopentyl-propionic acid methyl esterHCID 4622115797%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(4-bromo-phenyl)-3-cyclopentyl-propionic acid (1.37 g, 4.61 mmol) in methanol (23 mL) was treated slowly with 5 drops of concentrated sulfuric acid. The resulting reaction mixture was heated under reflux for 42 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), washed with 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, 19/1 hexanes/ethyl acetate) afforded 2-(4-bromo-phenyl)-3-cyclopentyl-propionic acid methyl ester (1.40 g, 97%) as a light yellow oil: EI-HRMS m/e calcd for C15H19BrO2 (M+) 310.0568, found 310.0569.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528543B1
Source datasetuspto-grants-2003_03
ORD IDord-1b10af1962a94ac58d60289e7b48c075
Source noteuspto-grants-2003_03