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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911330Generated: October 25, 2026

Carbon Tetrachloride → 2-Benzyl-6-bromomethyl-benzothiazole

https://huagongshe.com/reaction/911330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Benzyl-6-methyl-benzothiazoleHCID 50849889—
SolventChloroformHCID 6212—
Product2-Benzyl-6-bromomethyl-benzothiazoleHCID 5765655069%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-7a0dbd793abd41c6834be887afbe26d3
Source noteuspto-grants-2011_09