Reaktionsgleichung
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:11][CH3:12])=[C:6]([C@@H:8]([OH:10])[CH3:9])[CH:7]=1.FC1C=CC(OC)=C(C(=O)C)C=1.B(Cl)([C@@H]1[C@@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1)[C@@H]1[C@@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1.B(Cl)([C@H]1[C@H](C)C2C(C)(C)C(CC2)C1)[C@H]1[C@H](C)C2C(C)(C)C(CC2)C1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:11][CH3:12])=[C:6]([C@H:8]([OH:10])[CH3:9])[CH:7]=1Komponenten
5
Versuchsvorschrift
The title compound was prepared, according to the method used to make (S)-1-(5-fluoro-2-methoxy-phenyl)-ethanol from 1-(5-fluoro-2-methoxy-phenyl)-ethanone (see H. C. Brown, Tet. Letts., 35 (14), 2141-4, 1994) except that (+)-DIP-Chloride™ was used instead of (−)-DIP-Chloride™, as a white crystalline solid (63%).
Quellen und Nachweise
- ORD-Eintrag
- ord-b2b1310c2a664715a1645aa5e29b28c6
- Quelldatensatz
- uspto-grants-2014_12
- Patentnummer
- US08916593B2
Verknüpfte Notizen
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