関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-(2-(hydroxymethyl)phenyl)methanesulfonamide | HCID 22955815 | — |
| 触媒 | HCID 178418406 | HCID 178418406 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(Methylsulfonamido)benzaldehyde | HCID 11579304 | — |
反応手順
The title compound was synthesized according to the method described in WO 2008/073956 A2. To a solution of N-(2-(hydroxymethyl)phenyl)methanesulfonamide (3.44 g, 17.1 mmol) in anhydrous methylene chloride (68 mL) was added manganese dioxide (85% Aldrich, 17 g) and the mixture was stirred at ambient temperature overnight. Additional manganese dioxide (1.6 g) was added and the mixture stirred at 30° C. for 8 hours. The mixture was filtered through Celite, washing with methylene chloride, and the organic solution concentrated. The crude residue was purified by silica gel column chromatography (40-60% ethyl acetate in hexanes) to give a white solid (2.1 g, 62%). 1H NMR (CDCl3, 300 MHz) δ 10.59 (br s, 1H), 9.91 (s, 1H), 7.75-7.59 (m, 3H) 7.28-7.23 (t, 1H, J=7.5 Hz), 3.12 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09265772B2 |
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| 出典データセット | uspto-grants-2016_02 |
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| ORD ID | ord-0bc6a7ed187344eabab9d5f92a5e1981 |
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| 出典メモ | uspto-grants-2016_02 |
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