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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55771Generated: October 27, 2026

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

https://huagongshe.com/reaction/55771

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 numberUS09433614B2
Source datasetuspto-grants-2016_09
ORD IDord-195c3d7f9ab44d679c042dadfc5e6873
Source noteuspto-grants-2016_09