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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357739Generated: October 25, 2026

Methyl 3-bromothiophene-2-carboxylate → 3-Bromothiophene-2-carboxylic acid

https://huagongshe.com/reaction/357739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-bromothiophene-2-carboxylateHCID 2740074—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product3-Bromothiophene-2-carboxylic acidHCID 273968897.3%

Reaction Steps

3-Bromo-2-thiophenecarboxylic acid methyl ester (7.74 g) was dissolved in a mixture of methanol (35 ml) and tetrahydrofuran (35 ml), and 1N aqueous sodium hydroxide (53 ml) was added. The mixture was stirred at room temperature for 2 hours and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 3-bromo-2-thiophenecarboxylic acid (7.05 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840917
Source datasetuspto-grants-1998_11
ORD IDord-2e768a02cf3442ff911f2d68e5377a5c
Source noteuspto-grants-1998_11