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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

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-Tris((dimethylamino)methyl)phenolHCID 7026—
反応物Cesium carbonateHCID 10796—
反応物Ethyl 7-hydroxychromane-2-carboxylateHCID 11085381—
反応物1-(3-bromopropoxy)-4-phenoxy-2-propylBenzeneHCID 18772273—
生成物Ethyl 7-(3-(2-propyl-4-phenoxyphenoxy)propoxy)-chromane-2-carboxylateHCID 1877226676%

反応条件

温度70 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06645997B2
出典データセットuspto-grants-2003_11
ORD IDord-de6e3a706af54bc49ab9fde730dd9b1b
出典メモuspto-grants-2003_11