関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phenol | HCID 996 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Acridine-9-carboxylic acid | HCID 94721 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Thionyl Chloride | HCID 24386 | — |
| 生成物 | Phenyl acridine-9-carboxylate | HCID 517916 | — |
反応手順
Acridine-9-carboxylic acid (1 g, 4.1 mmol) was suspended in thionyl chloride (5 mL) and the reaction mixture was refluxed for 3 hours. The solvent was removed under reduced pressure leaving a yellow solid which was dissolved in methylene chloride and pyridine (350 μL) under argon. This solution was cooled in an ice bath and a solution of phenol (0.78 g, 8.2 mmol) in methylene chloride was added dropwise. The reaction mixture was stirred overnight at room temperature. After evaporation of solvent, the residue was redissolved in ethyl acetate and washed with water. The organic layer was dried over MgSO4 and concentrated to obtain a crudematerial which was chromatographed on silica gel (30% ethyl acetate/hexane)to yield the pure product as a yellow solid. 1H NMR (CDCl3) δ7.35-7.57 (m, 5H), 7.63-8.37 (m, 8H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05491072 |
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| 出典データセット | uspto-grants-1996_02 |
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| ORD ID | ord-18073fa1fa044b4ba7e65bd405adcda3 |
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| 出典メモ | uspto-grants-1996_02 |
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