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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48136Generated: October 25, 2026

Water → 4-{4-[4-(3-Cyano-propenyl)-benzyl]-phenyl}-but-3-enenitrile

https://huagongshe.com/reaction/48136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-ButenenitrileHCID 8009—
Reactant4,4'-Methylenebisbenzenediazonium bis(tetrafluoroborate)HCID 11732010—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
Product4-{4-[4-(3-Cyano-propenyl)-benzyl]-phenyl}-but-3-enenitrileHCID 5709159661%

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of 4,4′-methanediyl-bis-benzenediazonium tetrafluoroborate (11.9 g, 0.03 mol), prepared according to the method of example 6.1, allyl cyanide (8.05 g; 0.12 mol), and palladium acetate (0.135 g, 0.6 mmol) in 80 ml of ethanol is heated at 40° C. during 22 h. The heterogeneous reaction mixture is poured into 300 ml of water, extracted with ethyl acetate, washed with water, brine, dried over MgSO4, and evaporated. The crude beige product is recrystallized from 130 ml of ethanol, yielding 5.44 g (61%) of 4-{4-[4-(3-cyano-propenyl)-benzyl]-phenyl}-but-3-enenitrile as light beige crystals, melting point 128-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703182B1
Source datasetuspto-grants-2004_03
ORD IDord-7395024a17624351a2345a5625fb037c
Source noteuspto-grants-2004_03