HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitropropane → 4-Methyl-4-nitrovaleronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitropropane | HCID 398 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Catalyst | Hexadecyltrimethylammonium chloride | HCID 8154 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-Methyl-4-nitrovaleronitrile | HCID 3879140 | 64.6% |
Reaction Steps
Acrylonitrile (6.0 g, 113 mmol), 2-nitropropane (12.0 g, 135 mmol) and hexadecyltrimethyl ammonium chloride (2.0 g) were stirred in a 0.1N aqueous sodium hydroxide solution (200 ml) overnight at room temperature. The layers were separated and the aqueous layer was extracted twice with methylene chloride (50 ml). The combined organic layer was washed with saturated brine (30 ml). The solvent was evaporated and the residue was dried to give oily 4-methyl-4-nitrovaleronitrile (10.4 g, 73 mmol, yield 64.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148371B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-5876e68781f543829c661004d2c4b3bc |
| Source note | uspto-grants-2006_12 |