Sodium Carbonate → 4-amino-N-butylphthalimide

HRID 1633958

Reaktionsgleichung

Reaktionsgleichung von HRID 1633958
[CH2:1]([N:5]1[C:9](=[O:10])[C:8]2=[CH:11][C:12]([N+:15]([O-])=O)=[CH:13][CH:14]=[C:7]2[C:6]1=[O:18])[CH2:2][CH2:3][CH3:4].S(S([O-])=O)([O-])=O.[Na+].[Na+].C(=O)([O-])[O-].[Na+].[Na+]>CO.O>[CH2:1]([N:5]1[C:9](=[O:10])[C:8]2=[CH:11][C:12]([NH2:15])=[CH:13][CH:14]=[C:7]2[C:6]1=[O:18])[CH2:2][CH2:3][CH3:4]

Komponenten

6

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A solution of N-butyl-4-nitrophthalimide (1.45 g, 5.8 mmol) in methanol (30 mL) was added drop wise to a well stirred solution of sodium dithionite (6.50 g, 37.1 mmol) and sodium carbonate (3.22 g, 30.5 mmol) in water (40 mL), while the temperature was maintained at 70° C. After addition, heating at 70° C. was continued for a further 30 minutes, then the reaction mixture was allowed to cool to room temperature. The reaction volume was reduced to one third by rotary evaporation, and the residual water solution was extracted with diethyl ether (2×50 mL). The combined organic phases were dried with anhydrous Na2SO4, and then taken to dryness. The residual oil was recrystallised from ethanol/water to give 750 mg (59%) of N-butyl-4-aminophthalimide.

Aufarbeitung

  1. additionAfter addition
  2. temperatureheating at 70° C.
  3. temperatureto cool to room temperature
  4. customThe reaction volume was reduced to one third by rotary evaporation
  5. extractionthe residual water solution was extracted with diethyl ether (2×50 mL)
  6. dry with materialThe combined organic phases were dried with anhydrous Na2SO4
  7. customThe residual oil was recrystallised from ethanol/water

Quellen und Nachweise

ORD-Eintrag
ord-59cb9c93e6c0454e980d30d7a40fad3a
Quelldatensatz
uspto-grants-2003_01
Patentnummer
US06503949B1

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