Reaktionsgleichung
[O:1]1CCO[CH:2]1[C:6]1[CH:7]=[C:8]([CH:23]=[CH:24][CH:25]=1)[CH2:9][N:10]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][C:17]=2[O:19][CH2:20][C:21]#[N:22])[CH:12]=[CH:11]1>O1CCCC1.Cl.O>[CH:2]([C:6]1[CH:7]=[C:8]([CH:23]=[CH:24][CH:25]=1)[CH2:9][N:10]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][C:17]=2[O:19][CH2:20][C:21]#[N:22])[CH:12]=[CH:11]1)=[O:1]Komponenten
5
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
A solution of 1-[3-(1,3-dioxolan-2-yl)benzyl]-7-cyanomethoxyindole (50 mg., 0.15 mmol) in tetrahydrofuran (1 ml) and 2M hydrochloric acid (0.5 ml) was stirred at room temperature for 1 hour, diluted with water and extracted with ethyl acetate. The extract was dried and evaporated to a dark oil.
Aufarbeitung
- extractionextracted with ethyl acetate
- customThe extract was dried
- customevaporated to a dark oil
Quellen und Nachweise
- ORD-Eintrag
- ord-4eacd652e3ad4561be202fad9bfb3a9f
- Quelldatensatz
- uspto-grants-1994_01
- Patentnummer
- US05281593
Verknüpfte Notizen
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