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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022385Generated: October 30, 2026

Sulfuric Acid → (5-Bromo-4-fluoro-2-methyl-phenyl)-acetic acid methyl ester

https://huagongshe.com/reaction/1022385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium MethoxideHCID 10942334—
Reactant1-Bromo-2-fluoro-4-methyl-5-(2,2,2-trichloro-ethyl)-benzeneHCID 59614589—
SolventMethanolHCID 887—
Product(5-Bromo-4-fluoro-2-methyl-phenyl)-acetic acid methyl esterHCID 59614585—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 1-bromo-2-fluoro-4-methyl-5-(2,2,2-trichloro-ethyl)-benzene (29.2 g) in methanol (100 ml) is added a sodium methoxide solution (30% in methanol, 78.2 ml) dropwise. The reaction mixture is stirred at reflux for 24 hours, cooled to 5° C. and treated with concentrated sulfuric acid (13.2 ml) dropwise. After further warming to reflux for 21 hours, the mixture is concentrated and the residue diluted with water/ethyl acetate. The aqueous layer is extracted with ethyl acetate, the combined organic layers are washed with brine, dried over sodium sulfate and concentrated. The residue is purified by chromatography on silica gel (ethyl acetate/cyclohexane 1:3). Yield: 18.76 g of (5-bromo-4-fluoro-2-methyl-phenyl)-acetic acid methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722578B2
Source datasetuspto-grants-2014_05
ORD IDord-6381524a03d04d08a6ce5d06a44d1b80
Source noteuspto-grants-2014_05