HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenyl-1-propanone → 2-Amino-2-phenylbutanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenyl-1-propanone | HCID 7148 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | 2-Amino-2-phenylbutanenitrile | HCID 16794457 | 81% |
Reaction Steps
A mixture of propiophenone (30 g), KCN (34.5 g) and NH4Cl (30 g) in 180 mL of conc. NH4OH and 120 mL of EtOH is stirred at ambient temperature for 4 days. The reaction mixture is concentrated under vacuum and ether was added to the solid residue. The ether suspension is filtered and solid is washed with ether. Excess 1M of HCl in ether is added to the filtrate to precipitate HCl salt. The white solid is collected by filtration, washed with hexane and ether, and dried to give 29 g of the title compound as HCl salts. The white solid is basified with excess aqueous NaHCO3 and extracted with CH2Cl2. The extract is washed with brine, dried and concentrated to give 19 g of the titled compound as clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06413982B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-dd4c8eef2dfc45b0af29199d8030147c |
| Source note | uspto-grants-2002_07 |