Benzene → 3-Methyl-6-(morpholin-4-yl)-1-benzofuran-2(3H)-one

HRID 2295800Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2295800
[C:1]([O-:9])(=[O:8])[C:2]1C=CC=C[CH:3]=1.[NH2+:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1.O.[CH:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH3:3][CH:2]1[C:18]2[CH:19]=[CH:20][C:21]([N:10]3[CH2:15][CH2:14][O:13][CH2:12][CH2:11]3)=[CH:22][C:17]=2[O:9][C:1]1=[O:8]

Komponenten

4

Edukt 3

HCID 241BenzeneHCID 962WaterHCID 70501423Morpholinium benzoate

Produkt 1

HCID 135769393-Methyl-6-(morpholin-4-yl)-1-benzofuran-2(3H)-one

Versuchsvorschrift

A mixture of 18.2 g (0.1 mole) of 4-methyl-3-(3-oxobutyl)-maleic acid anhydride and 22 g (0.105 mole) of morpholinium benzoate in 400 ml of benzene is heated under reflux for 48 hours using a water separator. The benzene is removed in vacuo, the residue is taken up in methylene chloride and the organic phase is extracted twice with saturated sodium bicarbonate solution. The crude product remaining after drying and after removal of the methylene chloride is chromatographed over silica gel with petroleum ether/ether. Pale-yellow crystals are obtained, which are recrystallised from methylene chloride/ether. In this manner 3-methyl-6-morpholino-benzofuran-2(3H)-one having a melting point of 118°-121° C. is obtained.

Aufarbeitung

  1. temperatureis heated
  2. temperatureunder reflux for 48 hours
  3. customThe benzene is removed in vacuo
  4. extractionthe organic phase is extracted twice with saturated sodium bicarbonate solution
  5. customafter drying
  6. customafter removal of the methylene chloride
  7. customis chromatographed over silica gel with petroleum ether/ether
  8. customPale-yellow crystals are obtained
  9. customwhich are recrystallised from methylene chloride/ether

Quellen und Nachweise

ORD-Eintrag
ord-bef5894dd2f04cb8add4d1e021654d30
Quelldatensatz
uspto-grants-1984_01
Patentnummer
US04426380

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