4-Diethylamino-3-isopropylbenzaldehyde → 1-(4-Diethylamino-3-isopropylphenyl)prop-2-yn-1-ol
Reaktionsgleichung
[C:1]([Mg]Br)#[CH:2].C1COCC1.[CH2:10]([N:12]([CH2:24][CH3:25])[C:13]1[CH:20]=[CH:19][C:16]([CH:17]=[O:18])=[CH:15][C:14]=1[CH:21]([CH3:23])[CH3:22])[CH3:11]>>[CH2:24]([N:12]([CH2:10][CH3:11])[C:13]1[CH:20]=[CH:19][C:16]([CH:17]([OH:18])[C:1]#[CH:2])=[CH:15][C:14]=1[CH:21]([CH3:23])[CH3:22])[CH3:25]Komponenten
3
Versuchsvorschrift
In a manner analogous to example 1 e, the process is carried out by a reaction of 9.3 ml (4.7 mmol) of 0.5M ethynylmagnesium bromide/THF with 780 mg (3.5 mmol) of 4-diethylamino-3-isopropylbenzaldehyde. 720 mg of 1-(4-diethylamino-3-isopropylphenyl)prop-2-yn-1-ol are obtained in the form of a yellow oil (yield=83%).
Quellen und Nachweise
- ORD-Eintrag
- ord-852eb9d6920844f5aa413700470ec0e6
- Quelldatensatz
- uspto-grants-2012_04
- Patentnummer
- US08163952B2
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