Pyrazole → 1-tert-Butyl-1H-pyrazole
Reaktionsgleichung
[NH:1]1[CH:5]=[CH:4][CH:3]=[N:2]1.S(=O)(=O)(O)O.[C:11](O)([CH3:14])([CH3:13])[CH3:12]>>[C:11]([N:1]1[CH:5]=[CH:4][CH:3]=[N:2]1)([CH3:14])([CH3:13])[CH3:12]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 195 °C
Versuchsvorschrift
As in Example 2, the column was charged with 30 g of glass rings of diameter 3 mm, 16.4 g (0.24 mol) of pyrazole and 1.02 g (0.01 mol) of 96% by weight sulfuric acid, heated to 195° C. and reacted over the course of 7 hours with 703 g (9.5 mol) of tert-butanol vaporized at 180° C. 21.7 g of N-tert-butylpyrazole were obtained, boiling point 103° C., with a content of 99.4% (GC), which corresponds to a yield of 72.5%.
Aufarbeitung
- customvaporized at 180° C
Quellen und Nachweise
- ORD-Eintrag
- ord-738c381f04764410b3d0e79947f23b30
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05840913
Notizen zur Reaktion
Wird geladen…