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HRID 477831作成日:2026年10月27日

Sodium Bicarbonate → ethyl 4-[2-(N-ethoxycarbonyl-N-methylaminomethyl)morpholino]-2,3,5-trifluorobenzoylacetate

https://huagongshe.com/reaction/477831

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioateHCID 13564973—
反応物2-(N-ethoxycarbonyl-N-methylaminomethyl)morpholineHCID 14652577—
溶媒AcetonitrileHCID 6342—
生成物ethyl 4-[2-(N-ethoxycarbonyl-N-methylaminomethyl)morpholino]-2,3,5-trifluorobenzoylacetateHCID 14652581—

反応手順

A suspension of 3.36 g of diethyl 2,3,4,5-tetrafluorobenzoylmalonate, 2.22 g of 2-(N-ethoxycarbonyl-N-methylaminomethyl)morpholine and 0.84 g of sodium hydrogen carbonate in 13 ml of acetonitrile is refluxed for 5 hours., The reaction mixture is concentrated under reduced pressure, to the obtained residue is added 20 ml of chloroform and it is washed with water. After drying over anhydrous magnesium sulfate, the chloroform is distilled off under reduced pressure and to the residue are added 20 mg of p-toluenesulfonic acid and 20 ml of water. After refluxing for 16 hours, the resultant mixture is extracted with chloroform. The extract is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give ethyl 4-[2-(N-ethoxycarbonyl-N-methylaminomethyl)morpholino]-2,3,5-trifluorobenzoylacetate as an oily substance. The NMR values of this compound are identical with those of the compound obtained by Reference example 15(1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04889857
出典データセットuspto-grants-1989_12
ORD IDord-ee877af79de6461caa86cf2553f0fcab
出典メモuspto-grants-1989_12