Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230728Generated: October 30, 2026

Dimethylformamide → 2-Methoxy-5-(2-oxo-propoxy)-benzoic acid methyl ester

https://huagongshe.com/reaction/2230728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-hydroxy-2-methoxybenzoateHCID 12532676—
SolventEthyl AcetateHCID 8857—
Product2-Methoxy-5-(2-oxo-propoxy)-benzoic acid methyl esterHCID 70148846102.1%

Reaction Steps

Stir a mixture of methyl 4-hydroxy-2-methoxybenzoate (Danishefsky et al., J. Med. Chem. 1979, 101, 7001-7008, 0.54 g, 3 mmol), chloroacetone (6 mmol, Aldrich Chemical Company), potassium carbonate (9 mmol) and dimethylformamide at 50° C. overnight. Cool the reaction to room temperature, dilute with ethyl acetate, wash with saturated NaHCO3 solution and saturated brine. Dry (MgSO4) the organic phase, filter and concentrate the filtrate in vacuo. Purify the residue by column chromatography (silica gel, step gradient elution with 10% ethyl acetate in hexane to 30% ethyl acetate in hexane) and concentrate the appropriate fractions to afford 0.73 g of 2-methoxy-5-(2-oxo-propoxy)-benzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-1581841cd0e24037afa5288adb5d6351
Source noteuspto-grants-2002_07