Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414075Generated: October 25, 2026

Ammonia → 2-(2-Diisopropylamino ethyl) 3,3-dimethyl 2-(2-pyridyl) pentane-dinitrile

https://huagongshe.com/reaction/2414075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium amideHCID 24533—
Reactant3-Methyl-2-butenenitrileHCID 94301—
Reactant4-Diisopropylamino 2-(2-pyridyl)butyronitrileHCID 13319674—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-(2-Diisopropylamino ethyl) 3,3-dimethyl 2-(2-pyridyl) pentane-dinitrileHCID 54234562—

Reaction Conditions

Temperature-40 °C

Reaction Steps

The mixture of 4.7 g of sodium amide and 400 ml of liquid ammonia is cooled to -40° C., then the solution of 24.5 g of 4-diisopropylamino 2-(2-pyridyl) butane nitrile (Example 1a) in 30 ml of anhydrous ether is added, the temperature being maintained between -40° C. and -33° C. The mixture is stirred for 15 mins. at this temperature then the solution of 9 g of 3,3-dimethyl acrylonitrile in 40 ml of ether is added, still at the same temperature. The temperature is allowed to rise slowly up to ambient temperature (duration: about 5 hrs.). 200 ml of ether are added then water is added drop by drop. The ethereal phase is separated and the aqueous phase is re-extracted with ether. The ethereal extracts are collected and dried over sodium sulfate. The solvent is evaporated to dryness and the residue is chromatographed over a column of alumina with the eluting ethyl acetate-pentane (2.5-100) vol/vol mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04721710
Source datasetuspto-grants-1988_01
ORD IDord-b58ef02f0aaf4f5d8b614354929b82db
Source noteuspto-grants-1988_01