Diethyl Ether → HCID 178496926, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([C:7]([NH2:11])=[CH:8][C:9]=1[Cl:10])[CH:5]=O.C[C:13](C)([C:17]([O-:19])=[O:18])[C:14]([O-:16])=O.[CH2:21](OCC)C>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:7](=[CH:8][C:9]=1[Cl:10])[N:11]=[C:14]([OH:16])[C:13]([C:17]([O:19][CH3:21])=[O:18])=[CH:5]2Komponenten
4
Versuchsvorschrift
3,4-Dichloro-6-aminobenzaldehyde (2.85 g, 15 mmol) was stirred with dimethylmalonate (10 ml) at 140° C. for 20 h. The mixture was diluted with ethyl ether (100 ml). The precipitate was collected, washed twice with ethyl ether and dried in vacuo to give 2.86 g of methyl 6,7-dichloro-2-hydroxyquinoline-3-carboxylate.
Aufarbeitung
- customThe precipitate was collected
- washwashed twice with ethyl ether
- customdried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-23d4d49596454dcd92078d9946d5b5ab
- Quelldatensatz
- uspto-grants-1998_01
- Patentnummer
- US05710139
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