Acetic Acid → 2,2-Dimethyl-5-nitro-1,3-benzodioxole
Reaktionsgleichung
[N+:1]([O-:4])(O)=[O:2].C(O)(=O)C.[CH3:9][C:10]1([CH3:19])[O:14][C:13]2[CH:15]=[CH:16][CH:17]=[CH:18][C:12]=2[O:11]1>O>[CH3:9][C:10]1([CH3:19])[O:11][C:12]2[CH:18]=[CH:17][C:16]([N+:1]([O-:4])=[O:2])=[CH:15][C:13]=2[O:14]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 70% (conc.) nitric acid (20 ml) and glacial acetic acid (10 ml) cooled at 12° C. was treated by drops with 5 g (33.3 mmole) of the compound of Example 3A at a rate to maintain the temperature at 15°-20° C. Stirring was continued for 15 minutes after addition, then the brown slurry was diluted to 100 ml with water and filtered. The solid was washed with water, taken up in CH2Cl2, dried (Na2SO4) and evaporated to 5.40 g (83%) of pure yellow mononitro title compound.
Aufarbeitung
- temperatureto maintain the temperature at 15°-20° C
- additionafter addition
- filtrationfiltered
- washThe solid was washed with water
- dry with materialdried (Na2SO4)
- customevaporated to 5.40 g (83%) of pure yellow mononitro title compound
Quellen und Nachweise
- ORD-Eintrag
- ord-59ccbc6a7b29438d8b15da99e1c42378
- Quelldatensatz
- uspto-grants-1991_08
- Patentnummer
- US05037983
Notizen zur Reaktion
Wird geladen…