Pyridine → 4-Butylphenyl acetate
Reaktionsgleichung
[CH3:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:6]=[CH:7][C:8]([OH:11])=[CH:9][CH:10]=1.[CH3:12][C:13](OC(C)=O)=[O:14].N1C=CC=CC=1>ClCCl>[C:13]([O:11][C:8]1[CH:7]=[CH:6][C:5]([CH2:4][CH2:3][CH2:2][CH3:1])=[CH:10][CH:9]=1)(=[O:14])[CH3:12]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 10 g of 4-n-butylphenol, 10 ml of Ac2O and 8 ml of pyridine is stirred at reflux in 10 ml of dichloromethane. After 2 hours, the medium is cooled to room temperature, diluted with dichloromethane, washed with water, washed with 1M HCl solution, washed with saturated CuSO4 solution, washed with water and dried over MgSO4. After evaporation, 10.8 g of the expected compound are recovered in the form of an oil.
Aufarbeitung
- washwashed with water
- washwashed with 1M HCl solution
- washwashed with saturated CuSO4 solution
- washwashed with water
- dry with materialdried over MgSO4
- customAfter evaporation, 10.8 g of the expected compound
- customare recovered in the form of an oil
Quellen und Nachweise
- ORD-Eintrag
- ord-406b10465ee348928add84ae3d281821
- Quelldatensatz
- uspto-grants-2010_08
- Patentnummer
- US07777041B2
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