HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 5-Bromo-2-(bromomethyl)-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Bromo-2-methylbenzothiazole | HCID 3017457 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-Bromo-2-(bromomethyl)-1,3-benzothiazole | HCID 14458642 | — |
Reaction Steps
A mixture of 2-methyl-5-bromobenzothiazole (32.0 g), N-bromosuccinimide (25.1 g), carbon tetrachloride (700 ml) and a catalytic amount of benzoyl peroxide (0.2 g) was refluxed under irradiation by an UV lamp for 14 hours. The reaction mixture was cooled to room temperature, filtered to remove the precipitated succinimide and the filtrate was evaporated to dryness. The resulting solid was chromatographed over silica gel to obtain the product (7.8 g; m.p. 107° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04939140 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-68dea79663254e25a8d94dd5074b23f0 |
| Source note | uspto-grants-1990_07 |