Cyclohexene → (2-Amino-5-hydroxyphenyl)acetonitrile
Reaktionsgleichung
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([O:10]CC2C=CC=CC=2)=[CH:6][C:5]=1[CH2:18][C:19]#[N:20])([O-])=O.C1CCCCC=1>[Pd].C(O)C>[C:19]([CH2:18][C:5]1[CH:6]=[C:7]([OH:10])[CH:8]=[CH:9][C:4]=1[NH2:1])#[N:20]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A suspension of 5.4 g of 2-nitro 5-benzyloxyphenylacetonitrile, 5.4 ml of cyclohexene, 22 ml of ethanol and 3 g of 10% palladium on activated charcoal was refluxed for five hours. The suspension was then hot filtered and the filtrate evaporated. The residue was recrystallised from ethanol to produce dark beige crystals.
Aufarbeitung
- temperaturewas refluxed for five hours
- filtrationThe suspension was then hot filtered
- customthe filtrate evaporated
- customThe residue was recrystallised from ethanol
- customto produce dark beige crystals
Quellen und Nachweise
- ORD-Eintrag
- ord-9f85d6aa879d4d139c24221fd3f34af8
- Quelldatensatz
- uspto-grants-1997_12
- Patentnummer
- US05703266
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