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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625810Generated: November 1, 2026

6-Chloro-1-benzothiophene-2-carboxylic acid → 6-Chloro-1-benzothiophene

https://huagongshe.com/reaction/1625810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-1-benzothiophene-2-carboxylic acidHCID 7141919—
CatalystCopperHCID 23978—
SolventDiethyl EtherHCID 3283—
SolventQuinolineHCID 7047—
Product6-Chloro-1-benzothiopheneHCID 1239860175.2%

Reaction Steps

A solution of the above 6-chlorobenzo[b]thiophen-2-ylcarboxylic acid (3.0 g) and copper powder (1.2 g) in quinoline (20 ml) was stirred at 210° C. for 40 minutes. The mixture was cooled to room temperature and diluted with diethyl ether, and insoluble materials were filtered off. The filtrate was washed successively with 10% aqueous hydrochloric acid solution and brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane) to give 6-chlorobenzo[b]thiophene (1.79 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-acba3726e38c4cf994dd0a81839ed381
Source noteuspto-grants-2014_07