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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227451Generated: October 30, 2026

1-Phenyl-1-propanone → 2-Amino-2-phenylbutanenitrile

https://huagongshe.com/reaction/2227451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-1-propanoneHCID 7148—
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium ChlorideHCID 25517—
SolventEthanolHCID 702—
SolventAmmonium HydroxideHCID 14923—
Product2-Amino-2-phenylbutanenitrileHCID 1679445781%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413982B1
Source datasetuspto-grants-2002_07
ORD IDord-dd4c8eef2dfc45b0af29199d8030147c
Source noteuspto-grants-2002_07