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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Butenenitrile | HCID 8009 | — |
| Reactant | 4,4'-Methylenebisbenzenediazonium bis(tetrafluoroborate) | HCID 11732010 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-{4-[4-(3-Cyano-propenyl)-benzyl]-phenyl}-but-3-enenitrile | HCID 57091596 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06703182B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-7395024a17624351a2345a5625fb037c |
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| Source note | uspto-grants-2004_03 |
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