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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920252Generated: October 26, 2026

Bromoform → 5-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile

https://huagongshe.com/reaction/1920252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantTert-Butyl nitriteHCID 10906—
Reactant5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrileHCID 58500139—
Product5-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrileHCID 5850013339%

Reaction Steps

tert-Butyl nitrite (6.2 g, 0.060 mol) was added over a period of five minutes to solution of 5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile (6.60 g, 30.0 mmol) in bromoform (50 mL). After about ten minutes, an exotherm occurred, and the reaction was poured into ice water. The reaction temperature peaked at 55° C. The reaction was stirred at room temperature for 45 minutes and then concentrated under reduced pressure while heating at about 55° C. The crude product (20 g) was purified by column chromatography on silica gel (eluting sequentially with dichloromethane and 5% ethyl acetate in dichloromethane) to provide 3.37 g (39%) of 5-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168802B2
Source datasetuspto-grants-2012_05
ORD IDord-1e5eb36df7484d1b81be63192b09d8f7
Source noteuspto-grants-2012_05