1-(4-Chloro-pyridin-2-yl)-ethanone → 2-Acetyl-4-[1-(tert-butyldimethylsilyloxy)ethyl]pyridine
Reaktionsgleichung
[Si:1]([O:8][CH:9](C1C=CN=C(C#N)C=1)[CH3:10])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[C:19]([C:22]1[CH:27]=[C:26](Cl)[CH:25]=[CH:24][N:23]=1)(=[O:21])[CH3:20]>>[C:19]([C:22]1[CH:27]=[C:26]([CH:9]([O:8][Si:1]([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2])[CH3:10])[CH:25]=[CH:24][N:23]=1)(=[O:21])[CH3:20]Komponenten
3
Versuchsvorschrift
The title compound was prepared from 4-[1-(tert-butyldimethylsilyloxy)ethyl]-2-pyridinecarbonitrile according to the procedure for preparing 2-acetyl-4-chloropyridine described Example 33.
Quellen und Nachweise
- ORD-Eintrag
- ord-8011f74b46c341db845816c13b9aed65
- Quelldatensatz
- uspto-grants-2003_08
- Patentnummer
- US06608070B1
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