Potassium Carbonate → Methyl 2-benzylidene-3-hydroxypropionate

HRID 1066456

Reaktionsgleichung

Reaktionsgleichung von HRID 1066456
[CH:1](=[C:8]([CH2:13][O:14]C(=O)C)[C:9]([O:11][CH3:12])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+]>CO>[CH:1](=[C:8]([CH2:13][OH:14])[C:9]([O:11][CH3:12])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

4

Versuchsvorschrift

A crude product (5.99 g, 25.57 mmols) of methyl 2-benzylidene-3-acetoxypropionate was dissolved in 26 ml of methanol, and 3.53 g (25.5 mmols) of potassium carbonate were added thereto. The mixture was stirred at room temperature for 1 hour. Insoluble matters were separated by filtration, and the resulting solution was concentrated under reduced pressure. To the resulting residue were added 30 ml of water and 40 ml of toluene to extract an organic layer. The thus-obtained organic layer was washed with 30 ml of water and with 30 ml of a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified through silica gel column chromatography (silica gel 100 g, mixture of hexane and ethyl acetate at a ratio of from 3:1 to 2:1) to obtain 3.02 g (15.71 mmols) of the above title compound (yield: 61.4%).

Aufarbeitung

  1. customInsoluble matters were separated by filtration
  2. concentrationthe resulting solution was concentrated under reduced pressure
  3. additionTo the resulting residue were added 30 ml of water and 40 ml of toluene
  4. extractionto extract an organic layer
  5. washThe thus-obtained organic layer was washed with 30 ml of water and with 30 ml of a saturated aqueous solution of sodium chloride
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting residue was purified through silica gel column chromatography (
  9. additionsilica gel 100 g, mixture of hexane and ethyl acetate at a ratio of from 3:1 to 2:1)

Quellen und Nachweise

ORD-Eintrag
ord-71520c9e00c14b328c9dfc460987e2eb
Quelldatensatz
uspto-grants-2001_06
Patentnummer
US06242635B1

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