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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22914Generated: October 26, 2026

Acrylonitrile → 3-(4-Methoxyphenyl)prop-2-enenitrile

https://huagongshe.com/reaction/22914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantTriethylamineHCID 8471—
Reactant4-IodoanisoleHCID 69676—
ReactantTri-o-tolylphosphineHCID 80271—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
SolventPentaneHCID 8003—
SolventEthyl AcetateHCID 8857—
Product3-(4-Methoxyphenyl)prop-2-enenitrileHCID 3424059.5%

Reaction Steps

A solution of 4-iodoanisole (1 g, 4.2 mmol), acrylonitrile (0.3 ml, 4.7 mmol), tri-o-tolylphosphine (243 mg, 0.4 mmol), palladium (II) acetate (90 mg, 0.4 mmol) and triethylamine (1.78 ml, 12 mmol) in acetonitrile (20 ml) was refluxed under nitrogen for 14 hours. The reaction mixture was diluted with EtOAc (50 ml) and washed with 2M sodium hydrogen carbonate (100 ml), the organic layer was dried over magnessium sulphate and filtered. The filtrate was evaporated in vacuo and purified by column chromatography using pentane, then 95:5 pentane:ethyl acetate, then 90:10 pentane:ethyl acetate to give the title compound (414 mg, 2.5 mmol) as a mixture of cis and trans isomers as yellow crystals, 1H NMR (CDCl3 400 MHz) δ: 3.8 (s, 3H), 5.7 (d, 1H), 6.9 (d, 1H), 7.2 (d, 1H), 7.4 (d, 2H); LRMS: m/z 176 (M+NH4+); Anal. Found C, 74.44; H, 5.66; N, 8.36. C10H39NO.0.1H2O requires C, 74.42; H, 5.65; N, 8.41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849649B2
Source datasetuspto-grants-2005_02
ORD IDord-c1bd88a8906b45068f0e62552c375619
Source noteuspto-grants-2005_02