Methylamine → HCID 20273406, Verbindung
Reaktionsgleichung
[Cl:1][CH2:2][C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([S:12][C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][CH:14]=2)=[CH:8][CH:7]=1)=[O:4].[CH3:22][NH2:23]>C(O)C>[ClH:1].[CH3:22][NH:23][CH2:2][C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([S:12][C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][CH:14]=2)=[CH:8][CH:7]=1)=[O:4]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 3.0 g of 2-chloro-4'-(p-nitrophenylthio)acetanilide and a 4.0% aqueous solution of methylamine in ethanol was refluxed for 4 hours. The solvent was evaporated, the residue dissolved on dichloromethane and crystallized by the addition of hexane, giving 2.25 g of the desired product, mp 86°-89° C.
Aufarbeitung
- customThe solvent was evaporated
- dissolutionthe residue dissolved on dichloromethane
- customcrystallized by the addition of hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-36d51003b7674819b4c594c22681e699
- Quelldatensatz
- uspto-grants-1985_07
- Patentnummer
- US04532349
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