Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029816Generated: November 3, 2026

Toluene → 2-Amino-4-cyano-4-ethoxy-butyronitrile

https://huagongshe.com/reaction/1029816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHydrideHCID 166653—
Reactant2-Ethoxyprop-2-enenitrileHCID 12349940—
SolventWaterHCID 962—
Product2-Amino-4-cyano-4-ethoxy-butyronitrileHCID 19901181—

Reaction Conditions

Temperature-50 °C

Reaction Steps

51.5 millimoles of ethoxy-acrylonitrile are dissolved in 10 ml of anhydrous toluene at 60° C. under an argon atmosphere.77.25 millimole of a toluene solution 1.5M of diisobutyauminum hydride (51.5 ml) are added, dropwise, at -60° C. After stirring at this temperature for 45minutes, 7.7 m (.1 eq) of trimethylsilyl cyanide are added to the reaction mixture at -50° C. The latter is maintained at -50° C. for 3 hours while stirring, then hydrolyzed by ammonium chloride then water. After purification of the so-obtained aminonitrile, by liquid chromatography on silica (elution with ethyl acetate/ petroleum ether 1/1), 1.7 g of 2-amino-4-cyano-4-ethoxy-butyronitrile are obtained in a form of an orange-colored oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05103019
Source datasetuspto-grants-1992_04
ORD IDord-4ead34aa25bd44d7bb630ff7c7645e6d
Source noteuspto-grants-1992_04