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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487549Generated: October 26, 2026

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

https://huagongshe.com/reaction/487549

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 numberUS05296477
Source datasetuspto-grants-1994_03
ORD IDord-c640e292607543798d1c64df785a93de
Source noteuspto-grants-1994_03