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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372276Generated: October 30, 2026

Benzoyl Peroxide → 7-(Bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/1372276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant7-Methyl-1-benzothiopheneHCID 6428541—
SolventCarbon TetrachlorideHCID 5943—
Product7-(Bromomethyl)-1-benzothiopheneHCID 1075176138.6%

Reaction Steps

To a solution of intermediate 137, 7-methylbenzo[b]thiophene (1.0 g, 6.5 mmol) in CCl4 (20 mL) was added benzoyl peroxide (1.1 g, 4.54 mmol) followed by portionwise addition of NBS (1.15 g, 6.5 mmol). The reaction mixture stirred at reflux while irradiating with a 250 W lamp. The reaction mixture was stirred at reflux for 3 h. The solution was cooled, filtered and the solvent evaporated in vacuo. The residue was subjected to column chromatography on silica gel with hexanes as the eluent to afford the title compound (0.570 g, 33% yield): 1H NMR (400 MHz, CDCl3) δ: 7.80 (1H, dd, J=7.8, 1.7 Hz), 7.49 (1H, d, J=5.4 Hz), 7.40–7.33 (3H, m), 4.78 (2H, s). LCMS (M+H)+ m/z 209.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157447B2
Source datasetuspto-grants-2007_01
ORD IDord-10a4322af955426f9bdbbc8d25be25dd
Source noteuspto-grants-2007_01