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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987853Generated: November 3, 2026

Potassium Hydroxide → 6-Bromo-1-benzothiophene-2-carboxylic acid

https://huagongshe.com/reaction/1987853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant6-Bromo-benzo[b]thiophene-2-carboxylic acid methyl esterHCID 22474078—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-1-benzothiophene-2-carboxylic acidHCID 13567980—

Reaction Steps

A solution of 4.0 g (14.8 mmol) of methyl 6-bromo-1-benzothiophene-2-carboxylate in 40 ml of a 1:1 mixture of THF and 2 N potassium hydroxide solution is stirred at room temperature for 2 h. The solvent is removed in vacuo, and the residue is acidified with concentrated hydrochloric acid. The resulting precipitate is filtered off with suction, washed with water and dried in vacuo at 50° C. 3.55 g (93.5% of theory) of the desired product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553851B2
Source datasetuspto-grants-2009_06
ORD IDord-702988100c6c426ba6bb115f65669c49
Source noteuspto-grants-2009_06