Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4](OC)[C:3]=1[C:11]1[O:12][CH2:13][C:14]([CH3:17])([CH3:16])[N:15]=1.[F:18][C:19]1[CH:24]=[CH:23][C:22]([Mg]Br)=[CH:21][CH:20]=1.COC1C=CC=CC=1C1OCC(C)(C)N=1.COC1C=CC=CC=1[Mg]Br>>[Cl:1][C:2]1[C:3]([C:11]2[O:12][CH2:13][C:14]([CH3:17])([CH3:16])[N:15]=2)=[C:4]([C:22]2[CH:23]=[CH:24][C:19]([F:18])=[CH:20][CH:21]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1Komponenten
5
Edukt 4
Produkt 1
Versuchsvorschrift
By substituting equimolar amounts of 2-(2,4-dichloro-6-methoxyphenyl)-4,4-dimethyl-2-oxazoline and 4-fluorophenylmagnesium bromide for 2-(2-methoxyphenyl)-4,4-dimethyl-2-oxazoline and 2-methoxyphenylmagnesium bromide, the title compound was prepared following the procedure of Example 17, Step A, (85%), mp 93°-95° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-f8a353aafcc1481e86df9107b4a806d0
- Quelldatensatz
- uspto-grants-1987_12
- Patentnummer
- US04710513
Verknüpfte Notizen
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