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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586782Generated: October 27, 2026

N-bromobutanimide → 1-(4-Methylphenyl)-4-bromo-2-cyanopyrrole

https://huagongshe.com/reaction/1586782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-(4-Methylphenyl)pyrrole-2-carbonitrileHCID 2797715—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Methylphenyl)-4-bromo-2-cyanopyrroleHCID 1895625097.5%

Reaction Steps

To a solution of 1-(4-methylphenyl)pyrrole-2-carbonitrile (1.274 g) in tetrahydrofuran (25 ml) was added N-bromosuccinimide (1.776 g) in several portions at ambient temperature. After being stirred for 3 hours at the same temperature, the mixture was concentrated in vacuo. The residue was treated with diethyl ether. The precipitates were removed by filtration and washed with a small amounts of diethyl ether. The filtrates were concentrated in vacuo to give an oily residue, which was purified by silica gel column chromatography (elution by 40% dichloromethane in n-hexane) to yield 4-bromo-1-(4-methylphenyl)pyrrole-2-carbonitrile (1.78 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215994
Source datasetuspto-grants-1993_06
ORD IDord-cffdb142855e4730967cac0465f9bc82
Source noteuspto-grants-1993_06