Reaktionsgleichung
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C@@H:10]2[CH2:12][C@H:11]2[C:13]([OH:15])=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH2:16]([NH2:26])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]>>[CH2:16]([NH:26][C:13]([C@@H:11]1[CH2:12][C@H:10]1[C:7]1[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=1)=[O:15])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]Komponenten
3
Versuchsvorschrift
The title compound was prepared from trans-2-(4-nitrophenyl)cyclopropanecarboxylic acid and decylamine, substantially according to the procedure of Preparation 30. A 98% yield of a white, waxy solid, m.p. 127°-129° C., was obtained.
Aufarbeitung
- customsubstantially according to the procedure of Preparation 30
- customA 98% yield of a white, waxy solid, m.p. 127°-129° C., was obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-42ed8140793f4a5097acaf8f072ea660
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04343813
Verknüpfte Notizen
Wird geladen…