Reaktionsgleichung
[C:1]([O:10][CH3:11])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].CO[CH:14]1[CH2:18][CH2:17][CH:16](OC)O1>C(O)(=O)C>[N:4]1([C:3]2[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=2[C:1]([O:10][CH3:11])=[O:9])[CH:14]=[CH:18][CH:17]=[CH:16]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 500 g of methyl anthranilate and 438 g of 2,5-dimethoxytetrahydrofuran in 670 ml of glacial acetic acid is heated at reflux temperature for 11/2 hours. The acetic acid is then evaporated under reduced pressure and the residue is distilled to yield methyl 2-(1H-pyrrol-1-yl)-benzoate, b.p. 109°/0.1 mm Hg.
Aufarbeitung
- temperatureis heated
- temperatureat reflux temperature for 11/2 hours
- customThe acetic acid is then evaporated under reduced pressure
- distillationthe residue is distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-0bfb77e6bc12409ebf3689e5c4715367
- Quelldatensatz
- uspto-grants-1988_07
- Patentnummer
- US04758559
Verknüpfte Notizen
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