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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708419Generated: November 1, 2026

N-bromobutanimide → 4-(3-Cyano-2-thienyl)benzyl bromide

https://huagongshe.com/reaction/1708419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-(4-Methylphenyl)thiophene-3-carbonitrileHCID 20092836—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product4-(3-Cyano-2-thienyl)benzyl bromideHCID 2009285740.9%

Reaction Steps

24.5 g of 2-(4-methylphenyl)-3-cyanothiophene, prepared in E), are dissolved in 200 ml of carbon tetrachloride. 21.9 g of N-bromosuccinimide are added, as well as 0.1 g of benzoyl peroxide. The mixture is heated to reflux for 24 hours. The crystals of succinimide are filtered off and the solvent is evaporated off under vacuum. The residue is taken up in a mixture of hexane and ethyl acetate and the solution is kept in a freezer for 24 hours. The crystals formed are drained to give 14 g of 4-(3-cyano-2-thienyl)benzyl bromide in the form of crystals of melting point 80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05358950
Source datasetuspto-grants-1994_10
ORD IDord-ed3c5c127f314628911976e96671415d
Source noteuspto-grants-1994_10