Potassium Hydroxide → 4-(2,3-Dichlorophenyl)-1H-pyrrole-3-carboxylic acid
Reaktionsgleichung
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]1[C:10]([C:14]([O:16]CC)=[O:15])=[CH:11][NH:12][CH:13]=1.[OH-].[K+]>O>[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]1[C:10]([C:14]([OH:16])=[O:15])=[CH:11][NH:12][CH:13]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of ethyl 4-(2,3-dichlorophenyl)pyrrole-3-carboxylate (5.95 g, 21 mmol) and potassium hydroxide (6.5 g, 85%, 99 mmol) is heated at reflux for 6 hours, cooled, diluted with water and washed with diethyl ether. The aqueous phase is acidified with hydrochloric acid and filtered to obtain a solid. The solid is washed with diethyl ether and petroleum ether and dried to give the title product as a white solid (5.24 g) which is identified by 1H and 13C NMR spectral analyses.
Aufarbeitung
- temperatureis heated
- temperatureat reflux for 6 hours
- temperaturecooled
- washwashed with diethyl ether
- filtrationfiltered
- customto obtain a solid
- washThe solid is washed with diethyl ether and petroleum ether
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-7de814f62de34bd1b8e5fd555380480c
- Quelldatensatz
- uspto-grants-1995_02
- Patentnummer
- US05389669
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