Ethyl Acetate → 3'-(Octadecylcarbamoyloxy)acrylanilide
Reaktionsgleichung
C(OCC)(=O)C.[OH:7][C:8]1[CH:9]=[C:10]([CH:16]=[CH:17][CH:18]=1)[NH:11][C:12](=[O:15])[CH:13]=[CH2:14].[CH2:19]([N:37]=[C:38]=[O:39])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]>C(N(CC)CC)C>[CH2:19]([NH:37][C:38]([O:7][C:8]1[CH:9]=[C:10]([CH:16]=[CH:17][CH:18]=1)[NH:11][C:12](=[O:15])[CH:13]=[CH2:14])=[O:39])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
A reaction vessel is charged with 100 parts of ethyl acetate, 16.3 parts of 3'-hydroxyacrylanilide, 29.5 parts of octadecyl isocyanate and one part of triethylamine. The reaction mixture is heated at reflux for about 1 hour, cooled to 20°C and filtered. The solids are washed with ethyl acetate and air dried to give 40.5 parts of 3'-(octadecylcarbamoyloxy)acrylanilide, m.p. 124°-126°C.
Aufarbeitung
- temperatureThe reaction mixture is heated
- temperatureat reflux for about 1 hour
- filtrationfiltered
- washThe solids are washed with ethyl acetate and air
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-9baf46efd9c34029b085dac9484bcec8
- Quelldatensatz
- uspto-grants-1976_09
- Patentnummer
- US03979202
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