Ethyl bromoacetate → Ethyl (2-fluoro-4-trifluoromethyl-phenylamino)-acetate
Reaktionsgleichung
[F:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[NH2:12].Br[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16]>>[F:1][C:2]1[CH:7]=[C:6]([C:8]([F:10])([F:11])[F:9])[CH:5]=[CH:4][C:3]=1[NH:12][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16]Komponenten
3
Versuchsvorschrift
Prepared analogously to Example 165a starting from 2-fluoro-4-trifluoromethyl-phenylamine and ethyl bromoacetate. The crude product was purified by column chromatography (silica gel, gradient dichloromethane/MeOH 20:0→19:1).
Aufarbeitung
- customPrepared analogously to Example 165a
- customThe crude product was purified by column chromatography (silica gel, gradient dichloromethane/MeOH 20:0→19:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-2cabaa15feaf4d559437a962fb4cb190
- Quelldatensatz
- uspto-grants-2008_04
- Patentnummer
- US07351719B2
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