HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoform → 5-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile | HCID 58500139 | — |
| Product | 5-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile | HCID 58500133 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168802B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-1e5eb36df7484d1b81be63192b09d8f7 |
| Source note | uspto-grants-2012_05 |