Methanol → HCID 438674, Verbindung
Reaktionsgleichung
[NH2:1][CH:2]([C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[NH:10][CH:9]=1)[C:3]([O:5]CC)=[O:4].[OH-].[Na+].CO>C(O)(=O)C>[NH2:1][CH:2]([C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[NH:10][CH:9]=1)[C:3]([OH:5])=[O:4]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2 g of ethyl α-aminoindole-3-acetate, excess dilute NaOH solution, and a few mL of MeOH was stirred occasionally for 25 minutes. Since a solution had not been obtained, the mixture was heated on a steam bath for ten minutes. The resulting solution was allowed to stand at ambient temperature for 50 minutes. The solution was acidified with acetic acid. The solid which separated was collected by filtration and washed with H2O giving 1.50 g (86%) of the title compound as small buff plates, m.p. 217° (dec).
Aufarbeitung
- customSince a solution had not been obtained
- temperaturethe mixture was heated on a steam bath for ten minutes
- customThe solid which separated
- filtrationwas collected by filtration
- washwashed with H2O giving 1.50 g (86%) of the title compound as small buff plates, m.p. 217° (dec)
Quellen und Nachweise
- ORD-Eintrag
- ord-69fd0f6486c34ef8b949897a3d4dc910
- Quelldatensatz
- uspto-grants-1993_09
- Patentnummer
- US05245046
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