HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-(4-Methylphenyl)-4-bromo-2-cyanopyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-(4-Methylphenyl)pyrrole-2-carbonitrile | HCID 2797715 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Methylphenyl)-4-bromo-2-cyanopyrrole | HCID 18956250 | 97.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210092 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-16228395d2e24d60b1334358b0bece04 |
| Source note | uspto-grants-1993_05 |