Reaktionsgleichung
[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([OH:10])[C:3]=1[CH:4]=O.S(O)(O)(=O)=O.[NH2:16]O.C(Cl)Cl.C([O-])(O)=O.[Na+]>O>[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([OH:10])[C:3]=1[C:4]#[N:16]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2,6-dihydroxybenzaldehyde (300 mg, 2.17 mmol) and hydroxylamine sulfate (758 mg, 6.51 mmol) in water (30 mL) is stirred at RT for 45 min. Methylene chloride (60 mL) is added followed by NaHCO3 (911 mg, 10.85 mmol) and the mixture is stirred at RT for 30 min. The organic phase is separated and dried over sodium sulfate and the solvent removed under reduced pressure to give the title compound as a pale yellow solid.
Aufarbeitung
- stirringthe mixture is stirred at RT for 30 min
- customThe organic phase is separated
- dry with materialdried over sodium sulfate
- customthe solvent removed under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-debdfd5d2d5f45438a483499e7fa3ccd
- Quelldatensatz
- uspto-grants-2011_12
- Patentnummer
- US08084448B2
Verknüpfte Notizen
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