Water → N-Ethyl-4'-methylthio-2'-nitro-p-toluenesulfonanilide

HRID 1356675Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1356675
[H-].[Na+].[N+:3]([C:6]1[CH:22]=[C:21]([S:23][CH3:24])[CH:20]=[CH:19][C:7]=1[NH:8][S:9]([C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)(=[O:11])=[O:10])([O-:5])=[O:4].[CH2:25](I)[CH3:26].O>CN(C=O)C>[CH2:25]([N:8]([S:9]([C:12]1[CH:13]=[CH:14][C:15]([CH3:18])=[CH:16][CH:17]=1)(=[O:11])=[O:10])[C:7]1[CH:19]=[CH:20][C:21]([S:23][CH3:24])=[CH:22][C:6]=1[N+:3]([O-:5])=[O:4])[CH3:26]

Komponenten

6

Edukt 4

HCID 962WaterHCID 6340IodoethaneHCID 24758Sodium hydrideHCID 185093012'-Nitro-4'-methylthio-p-toluenesulfonanilide

Produkt 1

HCID 18509310N-Ethyl-4'-methylthio-2'-nitro-p-toluenesulfonanilideAusbeute 64,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a suspension of sodium hydride (65%, 0.21 g (5.76 mmol)) in 4.0 ml of DMF, 2′-nitro-4′-methylthio-p-toluenesulfonanilide (1.50 g (4.43 mmol)) was added with stirring at room temperature. To the resulting mixture, after 30 minutes' stirring at room temperature, ethyl iodide (0.52 ml (6.21 mmol)) was added dropwise and the mixture was stirred at room temperature for 16 hours. Then, the reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium bicarbonate, dilute hydrochloric acid, and saturated aqueous solution of sodium chloride successively. The ethyl acetate layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was then subjected to silica gel column chromatography with chloroform as eluent to give 1.04 g (64%) of the title compound as pale yellow crystals.

Aufarbeitung

  1. additionwas added
  2. stirringTo the resulting mixture, after 30 minutes' stirring at room temperature
  3. stirringthe mixture was stirred at room temperature for 16 hours
  4. extractionextracted with ethyl acetate
  5. washThe extract was washed with a saturated aqueous solution of sodium bicarbonate, dilute hydrochloric acid, and saturated aqueous solution of sodium chloride successively
  6. dry with materialThe ethyl acetate layer was dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-080e41be164a44c790283355840931f1
Quelldatensatz
uspto-grants-2003_07
Patentnummer
US06586617B1

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