関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Oxygen | HCID 977 | — |
| 反応物 | Methyl Acrylate | HCID 7294 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 3,4-Dimethoxyphenyl methyl ketone | HCID 14328 | — |
| 反応物 | HCID 178506586 | HCID 178506586 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | 5-(3,4-Dimethoxyphenyl)-5-methyl-dihydro-2-furanone | HCID 19369950 | — |
反応手順
100 ml of a 0.1 M solution of samarium(II) iodide in tetrahydrofuran is mixed, with oxygen carefully excluded, with the solution of 710 mg of 3,4-dimethoxyacetophenone, 500 mg of methyl acrylate and 350 mg of tert-butanol in 5 ml of tetrahydrofuran. The reaction solution is mixed thoroughly, allowed to stand for two hours at room temperature and then poured into 100 ml of 20% hydrochloric acid. It is stirred for two hours at room temperature and extracted with diethyl ether. The ether phase is washed with sodium thiosulfate solution and water, dried on sodium sulfate and concentrated by evaporation in a vacuum. The oily residue is chromatographed on a silica gel column (Kromasil 100/10 μm) with a hexane-tert-butyl methyl ether mixture (4:1). 570 mg of (R,S)-5-(3,4-dimethoxyphenyl)-5-methyl-dihydro-2-furanone is eluted, melting point 71.2° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06011060 |
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| 出典データセット | uspto-grants-2000_01 |
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| ORD ID | ord-2f2a8f24c2ce48d2844e84f48e2d08ed |
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| 出典メモ | uspto-grants-2000_01 |
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