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HRID 479632作成日:2026年10月26日
2,4,6-Tris((dimethylamino)methyl)phenol → Ethyl 7-(3-(2-propyl-4-phenoxyphenoxy)propoxy)-chromane-2-carboxylate
https://huagongshe.com/reaction/479632
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4,6-Tris((dimethylamino)methyl)phenol | HCID 7026 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Ethyl 7-hydroxychromane-2-carboxylate | HCID 11085381 | — |
| 反応物 | 1-(3-bromopropoxy)-4-phenoxy-2-propylBenzene | HCID 18772273 | — |
| 生成物 | Ethyl 7-(3-(2-propyl-4-phenoxyphenoxy)propoxy)-chromane-2-carboxylate | HCID 18772266 | 76% |
反応手順
To a 50 ml round-bottom flask were added ethyl 7-hydroxychromane-2-carboxylate (100 mg, 0.45 mmol), 4-(3-bromopropoxy)-3-propylphenyl phenyl ether (U.S. Pat. No. 6,008,237) (188 mg, 0.54 mmol), cesium carbonate (176 mg, 0.54 mmol), and DMF 3 ml. The resulting suspension was stirred at 70° C. for 5 hr. The solvent was removed under reduced pressure. The residue was diluted with AcOEt and water. The organic layer was separated. The aqueous layer was extracted twice with AcOEt. The combined organic layers were dried over anhydrous Na2SO4, filtered, concentrated, and chromatographed on silica gel. Eluting with 10% AcOEt/hexanes gave the title compound as a pale yellow oil 167 mg (76%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06645997B2 |
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| 出典データセット | uspto-grants-2003_11 |
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| ORD ID | ord-de6e3a706af54bc49ab9fde730dd9b1b |
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| 出典メモ | uspto-grants-2003_11 |
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