Sodium Acetate → HCID 68599246, Verbindung

HRID 1185503Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1185503
[CH2:1]([O:3][C:4](=[O:20])/[C:5](=[CH:12]/[C:13]1[CH:14]=[C:15]([CH3:19])[CH:16]=[CH:17][CH:18]=1)/[CH2:6][C:7]([O:9][CH2:10][CH3:11])=O)[CH3:2].C([O-])(=[O:23])C.[Na+]>C(OC(=O)C)(=O)C.O>[CH2:1]([O:3][C:4]([C:5]1[CH:6]=[C:7]([O:9][C:10](=[O:23])[CH3:11])[C:18]2[C:13](=[CH:14][C:15]([CH3:19])=[CH:16][CH:17]=2)[CH:12]=1)=[O:20])[CH3:2]

Komponenten

5

Versuchsvorschrift

To a solution of 2 g of 2-[1-m-Tolyl-meth-(E)-ylidene]-succinic acid diethyl ester in 10 ml of acetic acid anhydride, 594 mg sodium acetate was added and the reaction mixture was heated to reflux for 5 h. After cooling to RT the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic phases were washed three times with saturated aqueous sodium hydrogen carbonate solution. The organic phase was dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate (1/1). The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 860 mg.

Aufarbeitung

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 5 h
  3. extractionextracted with ethyl acetate
  4. washThe combined organic phases were washed three times with saturated aqueous sodium hydrogen carbonate solution
  5. dry with materialThe organic phase was dried over MgSO4
  6. customthe solvents were removed under reduced pressure
  7. customThe crude product was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate (1/1)
  8. additionThe fractions containing the product
  9. customthe solvent evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3e1f709694944f8c88086839924f237f
Quelldatensatz
uspto-grants-2014_03
Patentnummer
US08669266B2

Notizen zur Reaktion

Wird geladen…