Hydroxylamine → 3-Bromo-N-hydroxy-benzamidine
Reaktionsgleichung
[NH2:1][OH:2].[Br:3][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[C:7]#[N:8].C(=O)([O-])[O-].[K+].[K+]>CCO>[Br:3][C:4]1[CH:5]=[C:6]([C:7](=[N:1][OH:2])[NH2:8])[CH:9]=[CH:10][CH:11]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 120 °C
Versuchsvorschrift
Hydroxylamine (1.00 mL of a 50% aqueous solution, 16.3 mmol) was added to a solution of 3-bromobenzonitrile (750 mg, 4.12 mmol) and potassium carbonate (1.00 mg, 7.24 μmol) in EtOH (3.00 mL). The resulting mixture was heated to 120° C. in a sealed microwave vial for 40 min. After cooling to rt, the reaction mixture was concentrated in vacuo to afford the title compound i-3a. m/z (ES) 215 (MH)+.
Aufarbeitung
- temperatureAfter cooling to rt
- concentrationthe reaction mixture was concentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-86c4cd3d8d15446885678b8cdd4016b7
- Quelldatensatz
- uspto-grants-2013_02
- Patentnummer
- US08367679B2
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