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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909814Generated: November 4, 2026

N-bromobutanimide → 3-Bromo-7-(4-methylbenzyl)-1-benzothiophene

https://huagongshe.com/reaction/909814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-(4-Methylbenzyl)benzo[b]thiopheneHCID 67069100—
SolventAcetonitrileHCID 6342—
Product3-Bromo-7-(4-methylbenzyl)-1-benzothiopheneHCID 6706909156%

Reaction Steps

An acetonitrile (30 mL) solution of 7-(4-methylbenzyl)-1-benzothiophene (1.24 g, 5.20 mmol) was added with N-bromosuccinimide (1.01 g, 5.72 mmol) and stirred at room temperature for two hours. The solvent was evaporated under reduced pressure and diluted with ethyl acetate. After washed with 20 wt % sodium thiosulfate aqueous solution and brine, the organic phase was dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=100:1-50:1) to obtain a colorless powdered title compound (0.92 g, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017792B2
Source datasetuspto-grants-2011_09
ORD IDord-c843dfb426f6449ca4d7e941f4cfb55c
Source noteuspto-grants-2011_09