Methyl iodide → 2-[2(Methylamino)phenyl]-2-oxoethyl benzoate

HRID 358654Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 358654
IC.[C:3]([O:11][CH2:12][C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[NH2:21])=[O:14])(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:22](=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[C:3]([O:11][CH2:12][C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[NH:21][CH3:22])=[O:14])(=[O:10])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1

Komponenten

5

Versuchsvorschrift

Iodomethane (55.8 ml) was added to a stirred suspension of 2-(2-aminophenyl)-2-oxoethyl benzoate (109 g) and potassium carbonate (1 )8 g) in dry dimethylformamide (400 ml) at ambient temperature. The mixture was stirred at this temperature for 21hours and then at 40° for 5 hours. The solvent was removed under reduced pressure at 60°, water (100 ml) was added and the mixture extracted with dichloromethane (3×200 ml). The combined extracts were dried over sodium sulphate and the solvent was removed by evaporation to leave a dark oil. The oil was purified by flash chromatography on a silica gel column eluted with dichloromethane to give the novel compound 2-[2(methylamino)phenyl]-2-oxoethyl benzoate, m.p. 85°-87°.

Aufarbeitung

  1. waitat 40° for 5 hours
  2. customThe solvent was removed under reduced pressure at 60°
  3. additionwater (100 ml) was added
  4. extractionthe mixture extracted with dichloromethane (3×200 ml)
  5. dry with materialThe combined extracts were dried over sodium sulphate
  6. customthe solvent was removed by evaporation
  7. customto leave a dark oil
  8. customThe oil was purified by flash chromatography on a silica gel column
  9. washeluted with dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-b30bc81014514b848dcf8c36ca1eb807
Quelldatensatz
uspto-grants-1991_03
Patentnummer
US04997840

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