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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254042Generated: November 2, 2026

Bromoacetyl chloride → 3-Methyl-6-(bromoacetyl)benzothiazolinone

https://huagongshe.com/reaction/2254042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl chlorideHCID 89602—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantN-methylbenzothiazoloneHCID 20026384—
SolventDimethylformamideHCID 6228—
Product3-Methyl-6-(bromoacetyl)benzothiazolinoneHCID 86746657—

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. 33 g (0.20 mol) of 3-methylbenzothiazolinone 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 added 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 with water until the filtrate is neutral and dried. The product is recrystallized in 95° strength alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234924
Source datasetuspto-grants-1993_08
ORD IDord-f83669a1fe1d4c31ac42ea25a41b0ddf
Source noteuspto-grants-1993_08