関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Glycidyl tosylate, (R)- | HCID 154187 | — |
| 反応物 | 4'-Benzyloxy-2'-hydroxyacetophenone | HCID 309257 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-[4-Benzyloxy-2-((R)-1-oxiranylmethoxy)phenyl]ethanone | HCID 86644713 | 63.7% |
反応手順
To a stirred solution of 1-(4-(benzyloxy)-2-hydroxyphenyl)ethanone (3.36 g, 13.9 mmol) in anhydrous DMF (15 ml) was added NaH (0.62 g, 15.5 mmol). The mixture was allowed to stir at RT for 30 min, and a solution of (R)-oxiran-2-ylmethyl 4-methylbenzenesulfonate (3.17 g, 13.9 mmol) in DMF was added dropwise at RT. The mixture was slowly heated to 60° C. and stirred for 3 h. The reaction was quenched by addition of water (80 ml) and extracted three times with EtOAc. The combined organic layers were extracted twice with aq 1 M NaOH and washed with water and brine. The organic layer was dried with Na2SO4 and concentrated. The crude product obtained was purified by column chromatography with EtOAc/heptane (1:1) as eluent to afford the title compound (2.64 g) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08492549B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-24bdc5a905cc4c6c922bb2d0f51c2bc0 |
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| 出典メモ | uspto-grants-2013_07 |
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