Reaktionsgleichung
B.C1COCC1.C1(C)C=CC=CC=1.[Br:14][C:15]1[C:16]([O:29][CH3:30])=[C:17]([C:21](=[O:28])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH:18]=[CH:19][CH:20]=1>CO>[Br:14][C:15]1[C:16]([O:29][CH3:30])=[C:17]([C@@H:21]([OH:28])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH:18]=[CH:19][CH:20]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Under room temperature, a 1M borane THF solution (48 mL) was added to an R-CBS 1M toluene solution (1.20 mL). 1-(3-Bromo-2-methyloxyphenyl)heptane-1-one (7, 13 g) was added, and the mixture was stirred for 1 hour. Methanol was added, a solvent was distilled off, and the residue was purified, by chromatography to obtain (S)-1-(3-bromo-2-methyloxyphenyl)heptane-1-ol (8, 12.86 g, yield 75%).
Aufarbeitung
- distillationa solvent was distilled off
- customthe residue was purified, by chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-f970433cb798446ca67ec67d8996e9c2
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08889722B2
Verknüpfte Notizen
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