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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258397Generated: October 28, 2026

Chloroacetone → 2-Acetylbenzo[b]thiophene

https://huagongshe.com/reaction/258397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfideHCID 14804—
ReactantSulfurHCID 5362487—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Acetylbenzo[b]thiopheneHCID 8980574%

Reaction Steps

To a 200 ml four-necked flask, equipped with a stirrer, a thermometer and a reflux condenser, were added 11.7 g (150 m moles) of anhydrous sodium sulfide, 3.2 g (100 m moles) of sulfur and 100 ml of N-methylpyrrolidone, and the mixture was stirred at room temperature for one hour. To the reaction mixture was dropwise added 14.1 g (100 m moles) of 2-chlorobenzaldehyde, and the mixture was stirred at room temperature for 12 hours. To the reaction mixture, was dropwise added 11.1 g (120 m moles) of chloroacetone with cooling, and the reaction mixture was stirred at room temperature for 6 hours. After finishing the reaction, 100 ml of diethyl ether and 100 ml of water were added to the reaction mixture, and pH value of the aqueous layer was adjusted to higher than 11 with a sodium hydroxide aqueous solution, and extracted with diethyl ether. The diethyl ether extract was washed twice with water, and the diethyl ether layer was concentrated under a reduced pressure to obtain 13.0 g of 2-acetylbenzo[b]thiophene (yield 74%). Purity of the product was 95% as determined by gas chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266705
Source datasetuspto-grants-1993_11
ORD IDord-179d3449452b4e688d453a963c17d666
Source noteuspto-grants-1993_11