Reaktion #155650
ord-d7fb07ecdb1c478cb22023cf93ed5e08
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.DISSOLUTIONdissolves
- 2FiltrationThe precipitate (desired product) is filtered off
- 3Waschenwashed three times with diethyl ether
- 4Sonstigedried
- 5EinengenThe combined mother liquors are concentrated under reduced pressure
- 6Temperaturrefluxed for 13 h (the precipitate
- 7workup.DISSOLUTIONdissolves
- 8FiltrationThe precipitate (desired product) is filtered off
- 9Waschenwashed three times with diethyl ether
- 10Sonstigedried
Vorschrift
A suspension of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3(2H)-dione (A. Gutcait et al. Tetrahedron Asym. 1996, 7, 1641) (5.68 g, 27.9 mmol) and 4-(4-aminophenyl)-3-morpholinone (5.37 g, 27.9 mmol) in ethanol/water (9:1, 140 ml) is refluxed for 14 h (the precipitate dissolves, after some time again formation of a precipitate). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. The combined mother liquors are concentrated under reduced pressure and, after addition of a second portion of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3(2H)-dione (2.84 g, 14.0 mmol), suspended in ethanol/water (9:1, 70 ml) and refluxed for 13 h (the precipitate dissolves, after some time again formation of a precipitate). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. Total yield: 10.14 g, 92% of theory.