Reaktionsgleichung
[Br:1][CH2:2][C@H:3]([CH3:6])[CH2:4][OH:5].[C:7](OC(=O)C)(=[O:9])[CH3:8].O.C(OCC)(=O)C>N1C=CC=CC=1>[C:7]([O:5][CH2:4][C@@H:3]([CH3:6])[CH2:2][Br:1])(=[O:9])[CH3:8]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
6 g of (R)-(−)-3-bromo-2-methyl-1-propanol (39.2 mmol) were stirred in 6 ml of pyridine at room temperature. 4.08 g of acetic anhydride (43.1 mmol) were added and the reaction mixture was stirred for 4 h at 70° C. Stirring was continued for 16 h at room temperature. 40 ml of water and 60 ml of ethyl acetate were added to the reaction mixture. The organic layer was separated and washed with a further portion of water, then dried over magnesium sulfate, filtered, and evaporated under vacuum, whereby 6.03 g of the title compound were obtained.
Aufarbeitung
- stirringStirring
- waitwas continued for 16 h at room temperature
- customThe organic layer was separated
- washwashed with a further portion of water
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-6f9dc5e1502d4ada80fbc8054545cf17
- Quelldatensatz
- uspto-grants-2012_06
- Patentnummer
- US08202868B2
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