HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48136Erstellt: 24. Oktober 2026
Water → 4-{4-[4-(3-Cyano-propenyl)-benzyl]-phenyl}-but-3-enenitrile
https://huagongshe.com/de/reaction/48136
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 3-Butenenitrile | HCID 8009 | — |
| Edukt | 4,4'-Methylenebisbenzenediazonium bis(tetrafluoroborate) | HCID 11732010 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-{4-[4-(3-Cyano-propenyl)-benzyl]-phenyl}-but-3-enenitrile | HCID 57091596 | 61% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06703182B1 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-7395024a17624351a2345a5625fb037c |
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| Quellennotiz | uspto-grants-2004_03 |
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