Reaktionsgleichung
[C:1](Cl)(=[O:4])[CH:2]=[CH2:3].[C:6]1([NH2:12])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>C1COCC1>[C:6]1([NH:12][C:1](=[O:4])[CH:2]=[CH2:3])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Acryloyl chloride (28.5 mL; 350 mmol) was added to a stirred solution of phenylamine (30 mL; 320 mmol) and TEA (56 mL; 400 mmol) in THF (1 L) at 0° C. The reaction mixture was stirred for 3 h, poured onto brine and extracted with diethyl ether. The organic layer was dried, concentrated and recrystallized from hexane:EtOAc (3:1) to give the sub-title compound in a 79% yield.
Aufarbeitung
- additionpoured onto brine
- extractionextracted with diethyl ether
- customThe organic layer was dried
- concentrationconcentrated
- customrecrystallized from hexane:EtOAc (3:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-9dd75fc3027048f985b3ab018e1338b8
- Quelldatensatz
- uspto-grants-2001_09
- Patentnummer
- US06291475B1
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