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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163438Generated: October 31, 2026

Water → HCID 22751889, compound

https://huagongshe.com/reaction/2163438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenylacetonitrileHCID 8794—
Reactant3-(2-Chloroethyl)-3-azabicyclo[3.2.2]nonaneHCID 16146—
ReactantSodium amideHCID 24533—
SolventTolueneHCID 1140—
ProductHCID 22751889HCID 22751889—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 20 parts of α-phenylacetonitrile in 300 parts by volume of toluene is added 94 parts of 3-(2-chloroethyl)-3-azabicyclo[3.2.2]nonane dissolved in 500 parts by volume of toluene. The mixture is heated with stirring to about 80° C. and then 17 parts of sodium amide is added slowly over a period of 30 minutes. The mixture is heated at 80° C. for another 30 minutes and then cooled to room temperature. 500 Parts by volume of water is then added to the mixture and the organic layer separated and extracted with dilute hydrochloric acid. The aqueous acidic extract is made alkaline by the addition of dilute sodium hydroxide. The alkaline mixture is extracted with ether, the ether extract dried over calcium sulfate and distilled to afford 2-phenyl-4-(3-azabicyclo[3.2.2]non-3-yl)butyronitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134890
Source datasetuspto-grants-1979_01
ORD IDord-89dadc6389cc41349b50eb32dd9bf8d9
Source noteuspto-grants-1979_01