関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl 3-oxoglutarate | HCID 74591 | — |
| 反応物 | Lithium Bromide | HCID 82050 | — |
| 反応物 | 1,4-Dithiane-2,5-diol | HCID 98330 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | Methyl 2-(2-methoxy-2-oxoethyl)thiophene-3-carboxylate | HCID 58952963 | 82.4% |
反応手順
100.0 g of dimethyl 1,3-acetonedicarboxylate was dissolved in 2,800 ml of dioxane, and added thereto were 52.5 g of 2,5-dihydroxy-1,4-dithiane and 5.0 g of lithium bromide. The resulting mixture was refluxed for 15 hours, cooled to room temperature, and concentrated by evaporation. To the residue, 1,000 ml of n-hexane was added, stirred, and the hexane layer was separated. This extraction procedure was repeated twice using 500 ml portions of n-hexane. The separated n-hexane layers were combined and concentrated under reduced pressure to obtain 60.9 g (yield of 49%) of the title compound as an oil, which was directly used in the next step without any purification. An analytical sample of the title compound could be obtained by vacuum distillation.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07449580B2 |
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| 出典データセット | uspto-grants-2008_11 |
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| ORD ID | ord-e0ca6cd818a64c73aa1634761220ada2 |
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| 出典メモ | uspto-grants-2008_11 |
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