Reaktion #76188

Reaktionsgleichung

toluene

potassium carbonate

2-(5-Methyl-2-phenyl-4-oxazolyl)ethyl methanesulfonate

2-(5-methyl-2-phenyl-4-oxazolyl)ethyl methanesulfonate

compound [ 7 ]

2-(5-methyl-2-phenyl-4-oxazolyl)ethyl methanesulfonate

dimethyl 2-(4-hydroxybenzylidene)-malonate

compound [ 8 ]

dimethyl 2-(4-hydroxybenzylidene)malonate

→

title compound

Ausbeute 85.0%

dimethyl [4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene]-malonate

Ausbeute 85.0%

Lösungsmittel

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.DISSOLUTIONdissolved
2. 2
   Temperaturcooled
3. 3
   workup.STIRRINGby stirring
4. 4
   Sonstigethe aqueous layer was removed
5. 5
   workup.ADDITION10% aqueous sodium chloride solution (210 mL) was added to the organic layer
6. 6
   workup.STIRRINGwith stirring
7. 7
   Sonstigethe aqueous layer was removed
8. 8
   EinengenThe organic layer was concentrated
9. 9
   workup.DISSOLUTIONthe concentrated residue was dissolved in methanol (150 mL)
10. 10
    Temperaturunder heating
11. 11
    TemperaturThe reaction mixture was cooled to 10° C. or less
12. 12
    workup.STIRRINGthe reaction mixture was stirred for 1 hr
13. 13
    FiltrationThe obtained crystals were collected by filtration
14. 14
    Waschenwashed with methanol (65 mL)

Vorschrift

2-(5-Methyl-2-phenyl-4-oxazolyl)ethyl methanesulfonate obtained in Example 4 (compound [7]; 24.4 g) and dimethyl 2-(4-hydroxybenzylidene)-malonate obtained in Preparation Example 1 (compound [8]; 20.5 g) were mixed with tetrabutylammonium bromide (1.4 g) and toluene (210 mL). The mixture was heated to 90° C. and dissolved. Then potassium carbonate (13.2 g) was added and the mixture was stirred at 110° C. for 6 hr. The reaction mixture was ice-cooled and water (210 mL) was added, which was followed by stirring. After standing still, the aqueous layer was removed and 10% aqueous sodium chloride solution (210 mL) was added to the organic layer with stirring. The reaction mixture was allowed to stand and the aqueous layer was removed. The organic layer was concentrated and the concentrated residue was dissolved in methanol (150 mL) under heating. The reaction mixture was cooled to 10° C. or less and the reaction mixture was stirred for 1 hr. The obtained crystals were collected by filtration and washed with methanol (65 mL) to give the title compound (compound [9]; 31.1 g, yield 85.0%).

Quelle