関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl oxoacetate | HCID 70211 | — |
| 反応物 | 1-Methoxy-3-trimethylsilyloxy-1,3-butadiene | HCID 101051 | — |
| 触媒 | Zincchloride | HCID 3007855 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | Ethyl 4-oxo-3,4-dihydro-2H-pyran-2-carboxylate | HCID 22495097 | 75% |
反応手順
A solution of glyoxylic acid ethyl ester, polymer form (2.02 g, 8.9 mmol) and (3-methoxy-1 methylene-allyloxy)trimethylsilane (1.9 ml, 8.9 mmol, Danishefsky's diene) in benzene (12 ml) was placed under nitrogen. Zinc chloride (0.5 N in tetrahydrofuran, 8.9 ml, 4.45 mmol) was added and the reaction stirred at ambient temperature for 72 hours. The mixture was concentrated in vacuo, diluted with ethyl acetate (100 ml) and washed with 1 N hydrochloric acid (20 ml), saturated sodium bicarbonate (20 ml), and brine (20 ml). The organic layer was dried (Na2SO4), filtered, and the solvent evaporated in vacuo. The residue was purified by silica gel chromatography using a mixture of ethyl acetate/hexane (1:2) as eluent. Pure fractions were collected and the solvent evaporated in vacuo which afforded 1.2 g (75%) of 4-oxo-3,4-dihydro-2H-pyran-2-carboxylic acid ethyl ester as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07019026B1 |
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| 出典データセット | uspto-grants-2006_03 |
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| ORD ID | ord-92bd6faa833b4c6397d99a0800f07e7f |
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| 出典メモ | uspto-grants-2006_03 |
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