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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983384Generated: October 25, 2026

N-bromobutanimide → 5-(Bromomethyl)thiophene-2-carbonitrile

https://huagongshe.com/reaction/983384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methylthiophene-2-carbonitrileHCID 312733—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product5-(Bromomethyl)thiophene-2-carbonitrileHCID 1056001686.1%

Reaction Steps

A mixture of 5-methylthiophene-2-carbonitrile (9.9 g, 80.5 mmol), benzoylperoxide (0.23 g, 0.95 mmol), and N-bromosuccinimide (15 g, 84.3 mmol) in carbontetrachloride (200 mL) was heated at reflux for 6 h. The resulting suspension was filtered and the filtrate diluted with dichloromethane (400 mL), washed with a saturated sodium bicarbonate solution, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by column chromatography (EtOAc: n-hexane, 1:4) to give the title compound as a yellow oil (14.0 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864249B2
Source datasetuspto-grants-2005_03
ORD IDord-375028d805c444a8ab2f8e601bbaa48e
Source noteuspto-grants-2005_03