Dinitrobenzonitrile → 2-(5-(Tert-butyldimethylsilyloxy)pentyloxy)-6-nitrobenzonitrile
Reaktionsgleichung
[C:1]([Si:5]([CH3:14])([CH3:13])[O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][OH:12])([CH3:4])([CH3:3])[CH3:2].[N+:15]([C:18]1[CH:25]=[CH:24][CH:23]=[C:22]([N+]([O-])=O)[C:19]=1[C:20]#[N:21])([O-:17])=[O:16]>>[Si:5]([O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][O:12][C:22]1[CH:23]=[CH:24][CH:25]=[C:18]([N+:15]([O-:17])=[O:16])[C:19]=1[C:20]#[N:21])([C:1]([CH3:4])([CH3:3])[CH3:2])([CH3:14])[CH3:13]Komponenten
3
Versuchsvorschrift
Prepared as in Example 215c from 5-(tert-butyldimethyl-silyloxy)pentan-1-ol and 2,6-dinitrobenzonitrile as a pale yellow solid in 46% yield. MS 365 (MH+).
Quellen und Nachweise
- ORD-Eintrag
- ord-f43c4b804df44d46b4141a16e4f469ea
- Quelldatensatz
- uspto-grants-2014_01