Reaktionsgleichung
[CH2:1]([N:3]([CH2:13][CH3:14])[C:4](=[O:12])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[Cl:11])[CH3:2].[CH3:15][Si:16](Cl)([CH3:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH2:13]([N:3]([CH2:1][CH3:2])[C:4](=[O:12])[C:5]1[C:10]([Si:16]([CH3:23])([CH3:15])[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:9][CH:8]=[CH:7][C:6]=1[Cl:11])[CH3:14]Komponenten
3
Versuchsvorschrift
The title compound was prepared from the compound of Example e and 1.1 eq dimethylphenylsilyl chloride according to General Method A. Purification by HPLC with 1:9 ethyl acetate/hexanes gave 6.3 g of the desired product as a clear oil, a 91% yield.
Aufarbeitung
- customPurification by HPLC with 1:9 ethyl acetate/hexanes
Quellen und Nachweise
- ORD-Eintrag
- ord-2369a7a7151e4673a5f780d38ab28100
- Quelldatensatz
- uspto-grants-2000_10
- Patentnummer
- US06133252
Verknüpfte Notizen
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