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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104303Generated: October 30, 2026

4-Aminophenylacetonitrile → HCID 18765844, compound

https://huagongshe.com/reaction/2104303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenylacetonitrileHCID 77000—
SolventWaterHCID 962—
ProductHCID 18765844HCID 1876584434%

Reaction Steps

20 g (0.15 mol) of p-aminobenzyl cyanide, 19 ml (0.17 mol) of 2,5-dicetohexane and 2.88 g (0.015 mol) of hydrated p-toluene sulphonic acid are dissolved in a 500 ml flask. This mixture is heated to reflux, the water formed is trapped using a Dean Stark apparatus. At the end of the reaction, the solvent is evaporated off under vacuum and the residue is taken up in 300 ml of AcOEt. The organic solution is washed successively with twice 200 ml of water, 200 ml of a saturated solution of Na2CO3, 200 ml of water, 200 ml of a saturated solution of KHSO4 and finally 200 ml of water and 200 ml of brine. After drying over sodium sulphate, filtration and concentration under vacuum, the residue is purified rapidly on a silica column. A light beige solid is obtained with a yield of 34%. Melting point: 112-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576241B2
Source datasetuspto-grants-2009_08
ORD IDord-379e2a3ba00a4469aa3db66a43b6c2d2
Source noteuspto-grants-2009_08