Hydrochloric Acid → 1-tert-Butyl-1H-pyrazole
Reaktionsgleichung
Cl.[CH3:2][C:3]([NH:6][NH2:7])([CH3:5])[CH3:4].CO[CH:10](OC)[CH2:11][CH:12](OC)OC.Cl>C(O)C.CO>[CH3:2][C:3]([N:6]1[CH:12]=[CH:11][CH:10]=[N:7]1)([CH3:5])[CH3:4]Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of (1,1-dimethylethyl)hydrazine hydrochloride (1.02 g, 8.19 mmol) (Aldrich), 1,1,3,3-tetrakis(methyloxy)propane (1.344 g, 8.19 mmol) (Aldrich) and hydrochloric acid (0.672 ml, 8.19 mmol) in ethanol (10 ml) was heated under reflux. A solution formed. After 16 h the reaction had gone to completion and so was concentrated in vacuo to yield the crude product. This was dissolved in methanol and passed through an aminopropyl cartridge (20 g), eluting with methanol. The combined filtrates were concentrated in vacuo to yield the title compound as a cream gum (210 mg)
Aufarbeitung
- temperaturewas heated
- temperatureunder reflux
- customA solution formed
- concentrationso was concentrated in vacuo
- customto yield the crude product
- washeluting with methanol
- concentrationThe combined filtrates were concentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-c488f12d6c4a4cf9812dea55bb5b3fd5
- Quelldatensatz
- uspto-grants-2014_01
- Patentnummer
- US08633319B2
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