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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-methylbenzothiazolone | HCID 20026384 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methyl-6-(bromoacetyl)benzothiazolinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05296477 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-c640e292607543798d1c64df785a93de |
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| Source note | uspto-grants-1994_03 |
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