Reaktionsgleichung
[C:1]([NH2:6])(=[O:5])/[CH:2]=[CH:3]/[CH3:4].[CH2:7](Cl)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>CN(C)C=O>[CH2:7]([NH:6][C:1](=[O:5])/[CH:2]=[CH:3]/[CH3:4])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 200 ml of N,N-dimethylformamide, were added 17 g of crotonamide, 105 g of LEVATIT MP-500, which was also used in Example 68, and 32 g of benzylchloride. They were reacted at 50° C. for 4 hours with stirring. After the reaction, the reaction solution was treated in the same manner as in Example 69, the resulting distillation residue was recrystallized from benzine, and 25 of N-benzylcrotonamide having a melting point of 112.5°-113.6° C. was obtained (yield: 71%).
Aufarbeitung
- customThey were reacted at 50° C. for 4 hours
- customAfter the reaction
- additionthe reaction solution was treated in the same manner as in Example 69
- distillationthe resulting distillation residue
- customwas recrystallized from benzine, and 25 of N-benzylcrotonamide having a melting point of 112.5°-113.6° C.
- customwas obtained (yield: 71%)
Quellen und Nachweise
- ORD-Eintrag
- ord-0d5f89ffa64b4db3a7c5df88b628343f
- Quelldatensatz
- uspto-grants-1989_05
- Patentnummer
- US04835312
Verknüpfte Notizen
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