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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896489Generated: October 30, 2026

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

https://huagongshe.com/reaction/1896489

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 numberUS08518967B2
Source datasetuspto-grants-2013_08
ORD IDord-09c437a763804f3d9663ada70a1ba70c
Source noteuspto-grants-2013_08