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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864533Generated: October 30, 2026

Hydrochloric Acid → 5-Bromothiophene-3-carboxylic acid

https://huagongshe.com/reaction/1864533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 5-bromothiophene-3-carboxylateHCID 15293216—
CatalystWaterHCID 962—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Bromothiophene-3-carboxylic acidHCID 1203997892%

Reaction Steps

7.4 g (185 mmol) of sodium hydroxide pellets are added to a solution of 8.7 g (37 mmol) of ethyl 5-bromothiophene-3-carboxylate in 100 ml of tetrahydrofuran, 10 ml of methanol and a few drops of water. After stirring at room temperature for 18 hours, the reaction medium is taken up in ethyl acetate and washed with water. The aqueous phase obtained is acidified to pH 1 with aqueous hydrochloric acid solution and then extracted with dichloromethane. The organic phase obtained is dried over magnesium sulfate, filtered and concentrated under vacuum. 7 g (92%) of 5-bromothiophene-3-carboxylic acid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625914B2
Source datasetuspto-grants-2009_12
ORD IDord-a566a6e028174c5d81876df10d99b9dd
Source noteuspto-grants-2009_12