Sodium Carbonate → Ethyl 3-benzyl-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylate

HRID 54711Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 54711
[CH2:1]([N:8]1[C:13](=[O:14])[CH:12]2[CH:10]([CH:11]2[C:15]([OH:17])=[O:16])[C:9]1=[O:18])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.[C:20]1(C)C=CC(S(O)(=O)=O)=C[CH:21]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[CH2:1]([N:8]1[C:9](=[O:18])[CH:10]2[CH:12]([CH:11]2[C:15]([O:17][CH2:20][CH3:21])=[O:16])[C:13]1=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

5

Versuchsvorschrift

3-Benzyl-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylic acid (1.50 g, 6.13 mmol) was suspended in ethanol (30 ml), followed by adding p-toluenesulfonic acid monohydrate (145 mg, 0.76 mmol), heating the mixture under reflux for 8 hours, adding sodium carbonate to the reaction solution for neutralization, concentrating the mixture under reduced pressure, adding a saturated aqueous sodium bicarbonate to the reaction residue, extracting it with ethyl acetate, washing the extraction solution successively with water and saturated aqueous NaCl solution, drying it over anhydrous magnesium sulfate, concentrating the resulting solution to obtain ethyl 3-benzyl-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylate (1.51 g, 5.52 mmol, 90%), and recrystallizing it from ethanol to obtain a pure product.

Aufarbeitung

  1. temperatureheating the mixture
  2. temperatureunder reflux for 8 hours
  3. concentrationconcentrating the mixture under reduced pressure
  4. additionadding a saturated aqueous sodium bicarbonate to the reaction residue
  5. extractionextracting it with ethyl acetate
  6. washwashing the extraction solution successively with water and saturated aqueous NaCl solution
  7. dry with materialdrying it over anhydrous magnesium sulfate
  8. concentrationconcentrating the resulting solution

Quellen und Nachweise

ORD-Eintrag
ord-cfda687b248c4bf8a753c8ad23c1ad55
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05623078

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