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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1196504생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1196504

반응식

참여 물질

역할이름HCID투입량
반응물Acetic acid, 2-oxo-, methyl esterHCID 70205—
반응물1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 101051—
반응물benzyl N-(triphenyl-lambda5-phosphanylidene)carbamateHCID 10916618—
용매BenzeneHCID 241—
생성물2-Methyl 1-(phenylmethyl) 3,4-dihydro-4-oxo-1,2(2H)-pyridinedicarboxylateHCID 1512324270.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05114945
출처 데이터셋uspto-grants-1992_05
ORD IDord-f32ec5d30eec4850a80d99d97bf82b17
출처 메모uspto-grants-1992_05