Methyl hydrazidodicarboxylate → Bis(1-methoxy-2,2,6,6-tetramethylpiperidin-4-yl) Hydrazine-1,2-dicarboxylate
Reaktionsgleichung
[CH3:1][O:2][N:3]1[C:8]([CH3:10])([CH3:9])[CH2:7][CH:6]([OH:11])[CH2:5][C:4]1([CH3:13])[CH3:12].[NH:14]([C:20]([O:22]C)=O)[NH:15][C:16]([O:18][CH3:19])=[O:17]>CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-].[Ti+4]>[NH:15]([C:16]([O:18][CH:19]1[CH2:10][C:8]([CH3:9])([CH3:7])[N:3]([O:2][CH3:1])[C:4]([CH3:13])([CH3:12])[CH2:5]1)=[O:17])[NH:14][C:20]([O:11][CH:6]1[CH2:7][C:8]([CH3:9])([CH3:10])[N:3]([O:2][CH3:1])[C:4]([CH3:13])([CH3:12])[CH2:5]1)=[O:22]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a mixture of 15.8 g of 1-methoxy-2,2,6,6-tetramethylpiperidin-4-ol and 5.9 g of dimethyl hydrazine-1,2-dicarboxylate is added 1.4 g of tetrabutyl titanate at room temperature. The mixture is heated at 135°-145° C. for 12 hours and methanol is collected in a Dean-Stark trap. The reaction mixture is partitioned between toluene and water. The organic phase is then washed with water, brine, dried over anhydrous sodium sulfate and evaporated to leave 19.1 g of the crude desired product. Recrystallization of the crude product from acetonitrile affords 11.7 g of the title compound as an off-white solid; mp 147°-149° C.
Aufarbeitung
- temperatureThe mixture is heated at 135°-145° C. for 12 hours
- custommethanol is collected in a Dean-Stark trap
- customThe reaction mixture is partitioned between toluene and water
- washThe organic phase is then washed with water, brine
- dry with materialdried over anhydrous sodium sulfate
- customevaporated
- customto leave 19.1 g of the crude desired product
- customRecrystallization of the crude product from acetonitrile
Quellen und Nachweise
- ORD-Eintrag
- ord-3f169b14897446e38abb306a55f5528b
- Quelldatensatz
- uspto-grants-1995_11
- Patentnummer
- US05470980
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