関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | (3-Bromopropyl)benzene | HCID 12503 | — |
| 反応物 | 6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl ester | HCID 11845279 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carboxylic acid ethyl ester | HCID 11845282 | 85% |
反応手順
6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (2 g, 6.80 mmol), potassium carbonate (1.41 g, 10.194 mmol), and sodium iodide (200 mg, 1.359 mmol) were dissolved in dimethylformamide (100 ml). 1-Bromo-3-phenylpropane (2.01 ml, 13.59 mmol) was added thereto at room temperature, was stirred for 12 hours at 60° C., and washed with saturated ammonium chloride. The organic layer obtained by extracting the reaction mixture with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4) to obtain the title compound (yield 85%) as a dark red solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07741323B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-9f1d80b364074f929dd880780932bf51 |
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| 出典メモ | uspto-grants-2010_06 |
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