2-Butenoic acid, 4-oxo-, ethyl ester

反応条件: temp:0.00; pressure:0.00; stir:

反応条件: temp:0.00; pressure:0.00; stir:

反応条件: temp:22.01; pressure:0.00; stir:

反応条件: temp:0.00; pressure:0.00; stir:

反応条件: temp:0.00; pressure:0.00; stir:

反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

実験手順: A mixture of ethyl 4-oxobutenate (25.31 g), 2,3-butanedione-2-oxime (20.02 g) and 4N hydrogenchloride-ethyl acetate solution (300 mL) was stirred at room temperature for 4 days. After concentration of the reaction mixture, diethyl ether was added to the residue, and the residue was decanted and washed. Tetrahydrofuran (300 mL) was added to the residue, and thionyl chloride (35.33 g) was further added. The mixture was heated under reflux for 2 hrs. After concentration of the reaction mixture, ethyl acetate was added to the residue. The ethyl acetate layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give from a fraction eluted with ethyl acetate-hexane (1:8, v/v), ethyl (2E)-3-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)-2-propenoate as colorless crystals (24.98 g, yield 55%). Recrystallization from hexane gave prism crystals. melting point: 53-54° C. the residue was decanted washed Tetrahydrofuran (300 mL) was added to the residue, and thionyl chloride (35.33 g) was further added The mixture was heated under reflux for 2 hrs After concentration of the reaction mixture, ethyl acetate was added to the residue The ethyl acetate layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine dried over anhydrous magnesium sulfate concentrated to give from a fraction

反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

実験手順: A mixture of ethyl 4-oxobutenate (25.31 g), 2,3-butanedione-2-oxime (20.02 g) and 4N hydrogenchloride-ethyl acetate solution (300 mL) was stirred at room temperature for 4 days. After concentration of the reaction mixture, diethyl ether was added to the residue, and the residue was decanted and washed. Tetrahydrofuran (300 mL) was added to the residue, and thionyl chloride (35.33 g) was further added. The mixture was heated under reflux for 2 hrs. After concentration of the reaction mixture, ethyl acetate was added to the residue. The ethyl acetate layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give from a fraction eluted with ethyl acetate-hexane (1:8, v/v), ethyl (2E)-3-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)-2-propenoate as colorless crystals (24.98 g, yield 55%). Recrystallization from hexane gave prism crystals. melting point: 53-54° C. the residue was decanted washed Tetrahydrofuran (300 mL) was added to the residue, and thionyl chloride (35.33 g) was further added The mixture was heated under reflux for 2 hrs After concentration of the reaction mixture, ethyl acetate was added to the residue The ethyl acetate layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine dried over anhydrous magnesium sulfate concentrated to give from a fraction