HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-(4-(Bromomethyl)phenyl)benzo[d]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(4-Methylphenyl)-1,3-benzothiazole | HCID 919385 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(4-(Bromomethyl)phenyl)benzo[d]thiazole | HCID 13276729 | 67.4% |
Reaction Steps
To a solution of 45 g (0.2 mol) of 4-(benzothiazol-2-yl) toluene in 1000 ml of dry carbon tetrachloride were added 35.6 g (0.2 mol) of N-bromosuccinimide and a catalytic amount of benzoyl peroxide. The mixture was refluxed for 12 hours, and then allowed to cool down to room temperature. The precipitated succinimide was filtered off and the filtrate evaporated to dryness in vacuo, whereupon 55 g of crude crystals were obtained. Recrystallization from 1500 ml of cyclohexane gave 41 g of purified 4-(benzothiazol-2-yl) bromomethylbenzene as colorless flakes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232010 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-d62e145b728e4e42b4ad7a36cfd34c4b |
| Source note | uspto-grants-1980_11 |