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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487546Generated: October 26, 2026

Bromoacetyl chloride → 6-(Bromoacetyl)benzothiazolinone

https://huagongshe.com/reaction/487546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl chlorideHCID 89602—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantBenzothiazolinoneHCID 53400715—
SolventDimethylformamideHCID 6228—
Product6-(Bromoacetyl)benzothiazolinoneHCID 131717829—

Reaction Steps

210 g (1.60 mol) of aluminum chloride are introduced into a 500-cm3 ground-necked flask surmounted by a condenser, and 43 cm3 of dimethylformamide are then added dropwise and with magnetic stirring via a dropping funnel. 30.2 g (0.2 mol) of benzothiazolinone are then added and, while the reaction medium homogenizes, the temperature is stabilized at 70° C. using an oil bath. 19.8 cm3 (0.24 mol) of bromoacetyl chloride are then introduced gradually. After the addition, the mixture is left stirring for one hour at a temperature of 70° C. The reaction medium is hydrolyzed by pouring it onto crushed ice and the precipitate obtained is drained, washed copiously with water and dried. The product is recrystallized in dioxane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296477
Source datasetuspto-grants-1994_03
ORD IDord-39ce124092414e9da556882d13ff2e4c
Source noteuspto-grants-1994_03