関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-(2,5-Dimethoxy-phenyl)-1-(4-methoxy-phenyl)ethanone | HCID 358216 | — |
| 反応物 | Pyridinium chloride | HCID 10176127 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-(4-Hydroxy-phenyl)benzofuran-5-OL | HCID 656936 | 51% |
反応手順
A mixture of 74 (1.5 g, 5.2 mmol) and Pyridine HCl (10 g) was heated to 200° C. After 1.5 hr, the reaction was cooled and diluted with water. The aqueous layer was extracted with EtOAc and the organic layer was dried, concentrated to give a solid which was triturated with CH2Cl2 to give a solid (0.6 g, 51%): Mp=275–278° C.; 1H NMR (DMSO-d6) δ 9.81 (br s, 1 H), 9.12 (br s, 1 H), 7.66 (d, 2 H, J=2.5 Hz), 7.32 (d, 1 H, J=8.5 Hz), 7.00 (s, 1 H), 6.90–6.83 (m, 3 H), 6.65 (dd, 1 H, J=8.6 Hz, 2.6 Hz); MS 225 (M−H)−.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07022733B2 |
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| 出典データセット | uspto-grants-2006_04 |
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| ORD ID | ord-8f4f569ca48f43ba8ea62c03fde958a3 |
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| 出典メモ | uspto-grants-2006_04 |
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