HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 2-Benzyl-6-bromomethyl-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Benzyl-6-methyl-benzothiazole | HCID 50849889 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Benzyl-6-bromomethyl-benzothiazole | HCID 57656550 | 69% |
Reaction Steps
Combine 2-benzyl-6-methyl-benzothiazole (0.6 g, 2.51 mmol), NBS (0.5 g, 2.63 mmol), AIBN (40 mg, 0.25 mmol), carbon tetrachloride (10 mL) and reflux for 3 h. Cool the reaction mixture to ambient temperature, dilute with chloroform and wash with water. Dry the combined organic extracts over anhydrous Na2SO4, evaporate the solvent and purify by chromatography on silica gel eluting with hexane/EtOAc (1:0 and 9:1) to obtain the title compound as a white solid (0.2 g, 69%). MS (ES+) m/z: 319 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022062B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-7a0dbd793abd41c6834be887afbe26d3 |
| Source note | uspto-grants-2011_09 |