Reaktionsgleichung
[CH3:1][C:2]1([CH3:13])[CH2:11][C:10](=O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[O:3]1.Cl.[NH2:15][OH:16]>CO.N1C=CC=CC=1>[CH3:1][C:2]1([CH3:13])[CH2:11][C:10](=[N:15][OH:16])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[O:3]1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 82.5 °C
Versuchsvorschrift
A reaction mixture prepared from 10 mmol of 2,2-dimethyl-4-chromanone, 12 mmol of hydroxylamine hydrochloride in 5 ml of methanol and 5 ml of pyridine is heated with stirring over the course of 2 hours to 80-85° C., the solvent is distilled off on a rotary evaporator and the oily residue is crystallized under water.
Aufarbeitung
- temperatureis heated
- distillationthe solvent is distilled off on a rotary evaporator
- customthe oily residue is crystallized under water
Quellen und Nachweise
- ORD-Eintrag
- ord-8b926752e5bb4b5da7a24ab2bf4e3a79
- Quelldatensatz
- uspto-grants-2001_02
- Patentnummer
- US06191164B1
Verknüpfte Notizen
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