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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221082Generated: October 25, 2026

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

https://huagongshe.com/reaction/221082

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 numberUS08202984B2
Source datasetuspto-grants-2012_06
ORD IDord-1e6f21d8bdf547a6bed7715877d98e71
Source noteuspto-grants-2012_06