関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propanol | HCID 18669706 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propionaldehyde | HCID 22722409 | 83.6% |
反応手順
Sulfur trioxide pyridine complex (480 mg, 3.0 mmol) was added to a solution of 3-[3-(2-cyanophenylsulfonyloxy)-5-methylphenoxy]propanol (315 mg, 0.9 mmol), as prepared in the preceding step, N,N-diisopropylethylamine (0.5 mL, 3.9 mmol) and anhydrous dimethyl sulfoxide (0.2 mL, 2.8 mmol) in anhydrous dichloromethane (10 mL). The reaction mixture was stirred at ambient temperature for 1 hour and then quenched with 10% aqueous citric acid (30 mL). The mixture was extracted into dichloromethane (3×40 mL), and the dichloromethane solution was washed with 10% aqueous citric acid (30 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (dichloromethane) to give the title compound as a colorless oil (260 mg, 83%). 1H-NMR (300 MHz, CDCl3) δ 9.84 (s, 1H), 8.11 (m, 1H), 7.94 (m, 1H), 7.78-7.81 (m, 2H), 6.65 (s, 1H), 6.61 (s, 1H), 6.57 (s, 1H), 4.24 (t, J=6.0 Hz, 2H), 2.88 (t, J=6.0 Hz, 2H), 2.27 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05891909 |
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| 出典データセット | uspto-grants-1999_04 |
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| ORD ID | ord-b75a38a8c82c488299e6b949eded41fc |
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| 出典メモ | uspto-grants-1999_04 |
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