tert-Butylsulfinamide, (R)-(+)- → HCID 87426647, Verbindung
Reaktionsgleichung
[F:1][C:2]([F:16])([O:6][C:7]1[CH:8]=[C:9]([C:13](=O)[CH3:14])[CH:10]=[CH:11][CH:12]=1)[CH:3]([F:5])[F:4].[CH3:17][C:18]([S@:21]([NH2:23])=[O:22])([CH3:20])[CH3:19]>>[CH3:17][C:18]([S@:21]([NH:23][CH:13]([C:9]1[CH:10]=[CH:11][CH:12]=[C:7]([O:6][C:2]([F:16])([F:1])[CH:3]([F:5])[F:4])[CH:8]=1)[CH3:14])=[O:22])([CH3:20])[CH3:19]Komponenten
3
Versuchsvorschrift
The title compound is prepared in 81% yield (0.92 g, colorless oil) from 1-(3-(1,1,2,2-tetrafluoroethoxy)phenyl)ethanone (0.79 g, 3.36 mmol, Step-2) and (R)-2-methylpropane-2-sulfinamide by the similar manner in Step-4 of Amine-1.
Quellen und Nachweise
- ORD-Eintrag
- ord-7164bc71ce80479ba965299431e79cad
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09302991B2
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