Benzylamine → Acetoacetobenzylamide
Reaktionsgleichung
CC1(C)O[C:6](=[O:8])[CH:5]=[C:4]([CH3:9])[O:3]1.[CH2:11]([NH2:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C1(C)C=CC=CC=1>[CH2:11]([NH:18][C:6](=[O:8])[CH2:5][C:4](=[O:3])[CH3:9])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
9 ml (0.05 mol) of 2,2,6-trimethyl-4H-1,3-dioxin-4-one (diketene-acetone adduct) were added dropwise to a solution of 5.5 ml (0.05 mol) of benzylamine in 20 ml of toluene and the temperature was allowed to rise 70° C. The solution was refluxed for 2 h then the solvent was removed in vacuo. The crude product was triturated with ether obtaining 7.5 g of the title compound. M.p.=84°-86° C.
Aufarbeitung
- customto rise 70° C
- temperatureThe solution was refluxed for 2 h
- customthe solvent was removed in vacuo
- customThe crude product was triturated with ether obtaining 7.5 g of the title compound
Quellen und Nachweise
- ORD-Eintrag
- ord-f260c158922847e2b6dce05f84aaf68d
- Quelldatensatz
- uspto-grants-1998_03
- Patentnummer
- US05731322
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