Hydrazine hydrate (1:1) → 1-methylpiperidine-4-carbohydrazide
Reaktionsgleichung
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([C:8]([O:10]C)=O)[CH2:4][CH2:3]1.O.[NH2:13][NH2:14]>C(O)C>[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([C:8]([NH:13][NH2:14])=[O:10])[CH2:4][CH2:3]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 120 °C
Versuchsvorschrift
In a 25 mL sealed tube, methyl 1-methylpiperidine-4-carboxylate (0.2 g, 1.0 eq.) was dissolved in ethanol (5 mL) at RT. Hydrazine hydrate (0.127 g, 2 eq.) was introduced dropwise at RT and the reaction mixture was heated at 120° C. for 20 h. The reaction mixture was concentrated under reduced pressure (40° C., 20 mm Hg) to afford the crude 1-methylpiperidine-4-carbohydrazide (0.145 g) which was used without further purification in the following step.
Aufarbeitung
- customIn a 25 mL sealed tube
- concentrationThe reaction mixture was concentrated under reduced pressure (40° C., 20 mm Hg)
Quellen und Nachweise
- ORD-Eintrag
- ord-f580a074ce6e4ac2b2d43013fb0ffadf
- Quelldatensatz
- uspto-grants-2016_02
- Patentnummer
- US09266843B2
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