Methanol → Tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate
Reaktionsgleichung
[CH3:1][N:2]1[CH2:7][CH2:6][C:5](=[N:8][NH:9][C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:4][CH2:3]1.CC(C[AlH]CC(C)C)C.CO.O>C1COCC1>[CH3:1][N:2]1[CH2:3][CH2:4][CH:5]([NH:8][NH:9][C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:6][CH2:7]1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
To a solution of tert-butyl 2-(1-methylpiperidin-4-ylidene)hydrazinecarboxylate (500 mg, 2.20 mmol) in THF (50 mL) was added DIBAl-H (22 mL, 22 mmol) under nitrogen atmosphere. The resulting mixture was stirred at 25° C. overnight. Methanol (5 mL) was added to quench the reaction at −78° C. After being stirred at room temperature for 1 h, water (10 mL) was added. The solid was filtered off and washed with EtOAc. The combined filtrate was partitioned and extracted with EtOAc (3×50 mL), dried over Na2SO4, and concentrated. The residue was purified by silica gel chromatography eluting with EtOAc/petroleum ether (1:10) to give tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate (350 mg, 69% yield) as a colorless oil. LCMS (ESI) m/z: 230.4 [M+H+].
Aufarbeitung
- customto quench
- customthe reaction at −78° C
- stirringAfter being stirred at room temperature for 1 h
- filtrationThe solid was filtered off
- washwashed with EtOAc
- customThe combined filtrate was partitioned
- extractionextracted with EtOAc (3×50 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe residue was purified by silica gel chromatography
- washeluting with EtOAc/petroleum ether (1:10)
Quellen und Nachweise
- ORD-Eintrag
- ord-85c9a7c1b86540e0a58e0307bac4a0ed
- Quelldatensatz
- uspto-grants-2015_07
- Patentnummer
- US09090628B2
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