HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl chloride → 6-(Bromoacetyl)benzothiazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Benzothiazolinone | HCID 53400715 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(Bromoacetyl)benzothiazolinone | HCID 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 4 3cm3 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05268381 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-17f4936a96c24eb7850ebb475579ae41 |
| Source note | uspto-grants-1993_12 |