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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514548Generated: October 26, 2026

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

https://huagongshe.com/reaction/1514548

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. (3) The above 6-chlorobenzo[b]thiophene and 5-bromo-2-chlorobenzaldehyde obtained in Reference Example 16-(1) were treated in a manner similar to Reference Example 7 to give 5-bromo-2-chloro-1-(6-chlorobenzo[b]thiophen-2-ylmethyl)benzene as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222219B2
Source datasetuspto-grants-2012_07
ORD IDord-85e04b8dbc3d481aaf3b4e230b04b71f
Source noteuspto-grants-2012_07