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HRID 1196504作成日:2026年10月26日

Acetic acid, 2-oxo-, methyl ester → 2-Methyl 1-(phenylmethyl) 3,4-dihydro-4-oxo-1,2(2H)-pyridinedicarboxylate

https://huagongshe.com/reaction/1196504

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid, 2-oxo-, methyl esterHCID 70205—
反応物1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 101051—
反応物benzyl N-(triphenyl-lambda5-phosphanylidene)carbamateHCID 10916618—
溶媒BenzeneHCID 241—
生成物2-Methyl 1-(phenylmethyl) 3,4-dihydro-4-oxo-1,2(2H)-pyridinedicarboxylateHCID 1512324270.4%

反応手順

A solution of methyl glyoxylate (1.92 g) and (phenylmethyl) (triphenylphosphoranylidene)carbamate (6.00 g) in benzene (100 ml), was stirred at reflux under nitrogen, for 1 h. A solution of 1-methoxy-3-trimethylsilyloxybutadiene (5.00 g) in benzene (40 ml) was added and the resulting solution stirred at reflux, under nitrogen, for 18 h. The benzene was evaporated in vacuo, and the residue dissolved in tetrahydrofuran (100 ml), treated with 1M hydrochloric acid (10 ml) and stirred at 22° for 1 h. The solution was diluted with ethyl acetate (100 ml), water (40 ml) and the aqueous phase separated. The organic phase was washed with saturated aqueous sodium chloride, dried and evaporated. The residue was purified by chromatography eluting with ethyl acetate-hexane (1:1) to give the title compound as an oil (2.97 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05114945
出典データセットuspto-grants-1992_05
ORD IDord-f32ec5d30eec4850a80d99d97bf82b17
出典メモuspto-grants-1992_05