Reaktionsgleichung
[N+:1]([C:4]1[C:9]([N+:10]([O-:12])=[O:11])=[CH:8][CH:7]=[CH:6][C:5]=1[OH:13])([O-:3])=[O:2].Br[CH2:15][CH2:16][O:17][Si:18]([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19]>>[C:21]([Si:18]([O:17][CH2:16][CH2:15][O:13][C:5]1[CH:6]=[CH:7][CH:8]=[C:9]([N+:10]([O-:12])=[O:11])[C:4]=1[N+:1]([O-:3])=[O:2])([CH3:20])[CH3:19])([CH3:24])([CH3:23])[CH3:22]Komponenten
3
Versuchsvorschrift
tert-Butyl-[2-(2,3-dinitro-phenoxy)-ethoxy]-dimethyl-silane was prepared by a procedure according to example 108 (i) starting from 500 mg (2.72 mmol) 2,3-dinitro-phenol and 1.00 g (4.18 mmol) (2-Bromo-ethoxy)-tert-butyl-dimethyl-silane.
Quellen und Nachweise
- ORD-Eintrag
- ord-b73f6b5a3bf445309b73cd318c889108
- Quelldatensatz
- uspto-grants-2010_06
- Patentnummer
- US07741341B2
Verknüpfte Notizen
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