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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041218Generated: October 25, 2026

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

https://huagongshe.com/reaction/2041218

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 numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-94b9750b0db944a980c1313635c4ff93
Source noteuspto-grants-2013_11