Ammonium Hydroxide → Aminocinnamonitrile
Reaktionsgleichung
[C:1]([CH2:9][C:10]#[N:11])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH4+:12].[OH-]>>[NH2:12]/[C:1](/[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[CH:9]\[C:10]#[N:11]Komponenten
3
Versuchsvorschrift
A mixture of benzoylacetonitrile (510 mg, 3.51 mmol) and conc. NH4OH (4 mL, 56.0 mmol) in a sealed tube was stirred at 80 C for 20 h. After cooling, solids precipitated out, which were collected by filtration, dried on vacuum to give (Z)-3-amino-3-phenylacrylonitrile (95 mg).
Aufarbeitung
- temperatureAfter cooling
- customsolids precipitated out
- filtrationwhich were collected by filtration
- customdried on vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-bcfae22a18674aa9855e1cb7037bb801
- Quelldatensatz
- uspto-grants-2016_06
- Patentnummer
- US09359308B2
Notizen zur Reaktion
Wird geladen…