Ethanol → 2-Methylcyclopropanecarboxylic acid [1-(3-pyridinyl)propylidene]hydrazide
Reaktionsgleichung
[CH3:1][CH:2]1[CH2:4][CH:3]1[C:5]([NH:7][NH2:8])=[O:6].[CH2:9]([C:11]([C:13]1[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=1)=O)[CH3:10].CCO.CCCCCC.C(OCC)(=O)C>C(O)(=O)C.CCOCC>[N:15]1[CH:16]=[CH:17][CH:18]=[C:13]([C:11](=[N:8][NH:7][C:5]([CH:3]2[CH2:4][CH:2]2[CH3:1])=[O:6])[CH2:9][CH3:10])[CH:14]=1Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of 8.0 gm (0.07 mole) of 2-methylcyclopropanecarboxylic acid hydrazide, 9.46 gm (0.07 mole) of ethyl-3-pyridyl ketone, 10 drops of glacial acetic acid and 100 ml of EtOH was refluxed 20 hr. Tlc (9:1 Skellysolve B/Ethyl acetate on silica gel) shows no remaining starting material. The reaction mixture was cooled to room temperature and evaporated in vacuo to give a liquid. The liquid solidified on standing. The solid was slurried in ether, collected and dried to give 4.77 gm (29%) of the title compound having a melting point of 137.3° C.
Aufarbeitung
- temperaturewas refluxed 20 hr
- customevaporated in vacuo
- customto give a liquid
- customcollected
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-2754237dc1a7450f85f102c2acdfdd41
- Quelldatensatz
- uspto-grants-1991_06
- Patentnummer
- US05023334
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