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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727244Generated: November 2, 2026

N-bromobutanimide → 2-(Bromomethyl)-5-methoxy-1,3-benzothiazole

https://huagongshe.com/reaction/1727244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methoxy-2-methylbenzothiazoleHCID 76252—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-5-methoxy-1,3-benzothiazoleHCID 53440846—

Reaction Steps

2.58 g (14.5 mmol; 1.3 eq.) of N-bromosuccinimide and a spatula tip's worth of aza-bis-isobutyronitrile are added to 2 g (11.16 mmol) of 2-methyl-5-methoxy-1,3-benzothiazole in solution in 25 ml of anhydrous carbon tetrachloride. The reaction mixture is heated under reflux and under irradiation for 6 hours, with a spatula tip's worth of aza-bis-isobutyronitrile added every 2 hours. After returning to ambient temperature, the insoluble part formed is filtered, the solvent is evaporated off under reduced pressure and the residue is purified by chromatography on a silica column (eluent: ethyl acetate/heptane 1/4). The expected product is obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495021B2
Source datasetuspto-grants-2009_02
ORD IDord-c3f7ff6a1a0b462dbe379fc02e73aed8
Source noteuspto-grants-2009_02