Malonic Acid → 3-(2-Bromo-5-nitrophenyl)prop-2-enoic acid
Reaktionsgleichung
[Br:1][C:2]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:3]=1[CH:4]=O.C(O)(=O)[CH2:14][C:15]([OH:17])=[O:16].N1CCCCC1>N1C=CC=CC=1>[Br:1][C:2]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:3]=1[CH:4]=[CH:14][C:15]([OH:17])=[O:16]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
This reaction was carried out similarly to Example 1, with 2-bromo-5-nitrobenzaldehyde and malonic acid in pyridine and with piperidine. The product of melting point 185° C, was obtained in 57% yield.
Aufarbeitung
- customThe product of melting point 185° C, was obtained in 57% yield
Quellen und Nachweise
- ORD-Eintrag
- ord-15a25f359fbd49eba28b49004fd031d8
- Quelldatensatz
- uspto-grants-1993_08
- Patentnummer
- US05237089
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