Methyl 3-bromo-5-hydroxybenzoate → Methyl 3-bromo-5-[2-chloro-4-(ethylsulfonyl)phenoxy]benzoate
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([OH:12])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].[CH2:13]([S:15]([C:18]1[CH:23]=[CH:22][C:21](F)=[C:20]([Cl:25])[CH:19]=1)(=[O:17])=[O:16])[CH3:14]>>[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([O:12][C:21]2[CH:22]=[CH:23][C:18]([S:15]([CH2:13][CH3:14])(=[O:17])=[O:16])=[CH:19][C:20]=2[Cl:25])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]Komponenten
3
Versuchsvorschrift
The subtitle compound was prepared as described in example 2 step (iii) but instead using the product from step (i) and the product from example 3 step (i).
Quellen und Nachweise
- ORD-Eintrag
- ord-3ddf4ae7547741d69ddd3fe4438b4feb
- Quelldatensatz
- uspto-grants-2012_04
- Patentnummer
- US08148572B2