関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 1-(p-Chlorophenyl)acetone | HCID 79699 | — |
| 反応物 | (E)-3-(2-naphthyl)-2-propenyl bromide | HCID 22252145 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (E)-3-(4-chlorophenyl)-6-(2-naphthyl)-5-hexen-2-one | HCID 19038600 | 78% |
反応手順
2.56 g of p-chlorophenylacetone was dissolved in a mixed solution of 5 ml of dimethylformamide and 5 ml of benzene, and a dimethylformamide 8 ml/benzene 8 ml solution containing 0.62 g of 60% oily sodium hydride and 3.50 g of (E)-3-(2-naphthyl)-2-propenyl bromide, was added under cooling with ice with stirring, followed by stirring at room temperature for 2 hours. The reaction solution was acidified by an addition of 1N hydrochloric acid and extracted by an addition of water and ethyl ether. Then, the organic layer was washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The drying agent was filtered off, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=5/1) to obtain 3.70 g of the above-identified compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05643958 |
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| 出典データセット | uspto-grants-1997_07 |
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| ORD ID | ord-397ef8e10d194d67a54872cfd2b6b3e6 |
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| 出典メモ | uspto-grants-1997_07 |
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