関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Methyl-2-phenylpropanal | HCID 283879 | — |
| 反応物 | 2,2-Dimethyl-3-phenyloxirane | HCID 5743355 | — |
| 反応物 | (S)-4-methylbenzenesulfinamide | HCID 11116285 | — |
| 触媒 | Titanium tetraethoxide | HCID 76524 | — |
| 触媒 | Tris(pentafluorophenyl)borane | HCID 582056 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | (S)-N-(2-Methyl-2-phenylpropylidene)-p-toluenesulfinamide | HCID 69625671 | 81% |
反応手順
To a stirred solution of 2.5 g of 2,2-dimethyl-3-phenyloxirane (16 mmol) in 85 mL of anhydrous benzene is added 0.415 g (0.362 mmol, 5 mol %) of tris(pentafluorophenyl) borane. The light yellow solution is stirred at 25° C. for 19 hours. The reaction mixture containing the 2-methyl-2-phenylpropanal is then treated with (S)-p-toluenesulfinamide (2.3 g, 15 mmol) followed by a solution of 16 mL (73 mmol) titanium ethoxide in 155 mL of benzene. The yellow solution is stirred at 25° C. for 24 hours then cooled to 5-10° C. and quenched with 245 mL of water. The mixture is filtered through diatomaceous earth, and the filter cake washed with methylene chloride (4×50 mL). The aqueous layer is washed with methylene chloride (1×25 mL). The combined organic layers are dried (MgSO4) and concentrated under reduced pressure to give 3.74 g (81%) of the desired product as a white solid. The product is used without further purification in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06951955B2 |
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| 出典データセット | uspto-grants-2005_10 |
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| ORD ID | ord-a21d45c9fa064fad827402ad2f202479 |
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| 出典メモ | uspto-grants-2005_10 |
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