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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Acetic acid, 2-oxo-, methyl ester | HCID 70205 | — |
| 反応物 | 1-Methoxy-3-trimethylsilyloxy-1,3-butadiene | HCID 101051 | — |
| 反応物 | benzyl N-(triphenyl-lambda5-phosphanylidene)carbamate | HCID 10916618 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 2-Methyl 1-(phenylmethyl) 3,4-dihydro-4-oxo-1,2(2H)-pyridinedicarboxylate | HCID 15123242 | 70.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05114945 |
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| 出典データセット | uspto-grants-1992_05 |
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| ORD ID | ord-f32ec5d30eec4850a80d99d97bf82b17 |
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| 出典メモ | uspto-grants-1992_05 |
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