Trifluoroacetic acid → Ethyl 4-[15-(trifluoromethyl)pentadecylamino]benzoylacetate
Reaktionsgleichung
[F:1][C:2]([F:41])([F:40])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH:18][C:19]1[CH:39]=[CH:38][C:22]([C:23]([CH:25](C(OCC)=O)[C:26]([O:28][C:29](C)(C)[CH3:30])=[O:27])=[O:24])=[CH:21][CH:20]=1.FC(F)(F)C(O)=O.[OH-].[K+]>>[F:1][C:2]([F:40])([F:41])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH:18][C:19]1[CH:39]=[CH:38][C:22]([C:23]([CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27])=[O:24])=[CH:21][CH:20]=1Komponenten
4
Versuchsvorschrift
A solution of 3.0 g. of tert-butyl ethyl 4-[15-(trifluoromethyl)pentadecylamino]benzoylmalonate and 10 ml. of trifluoroacetic acid is warmed with stirring for 3 hours. The solution is poured onto ice and neutralized with potassium hydroxide. The resulting precipitate is collected by filtration, washed with water and dried. Recrystallization from chloroform affords the product as a white solid.
Aufarbeitung
- filtrationThe resulting precipitate is collected by filtration
- washwashed with water
- customdried
- customRecrystallization from chloroform
Quellen und Nachweise
- ORD-Eintrag
- ord-2d6f49e8b7784cdca120d95b537d4ede
- Quelldatensatz
- uspto-grants-1981_12
- Patentnummer
- US04305959
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