Reaktionsgleichung
[CH2:1]([O:3][CH:4]([O:13][CH2:14][CH3:15])[C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)[CH3:2].C[CH2:17][O:18]CC>>[CH2:1]([O:3][CH:4]([O:13][CH2:14][CH3:15])[C:5]1[CH:12]=[CH:11][C:8]([CH2:9][CH2:17][OH:18])=[CH:7][CH:6]=1)[CH3:2]Komponenten
3
Versuchsvorschrift
To a solution of 4-(diethoxymethyl)benzaldehyde (5.0 g, 24 mmol) in ether (65 ml), cooled to -10° C., was added dropwise a 1.5M toluene-THF methylmagnesium bromide solution (64 ml, 96 mmol) at such a rate that the temperature remains below 0° C. After the addition the reaction was quenched with saturated ammonium chloride (80 ml) and the solution was diluted with water (50 ml) and extracted with ether (2×75 ml). The combined extracts were washed with water (50 ml) and brine (50 ml), dried over sodium sulfate and concentrated in vacuo, leaving present title product (5.2 g, 97%) as an oil.
Aufarbeitung
- customremains below 0° C
- additionAfter the addition the reaction
- customwas quenched with saturated ammonium chloride (80 ml)
- additionthe solution was diluted with water (50 ml)
- extractionextracted with ether (2×75 ml)
- washThe combined extracts were washed with water (50 ml) and brine (50 ml)
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-f5047be61d054797ad1324dbbb4741ef
- Quelldatensatz
- uspto-grants-1991_10
- Patentnummer
- US05061717
Verknüpfte Notizen
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