참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-(p-Chlorophenyl)acetone | HCID 79699 | — |
| 반응물 | (E)-3-(2-naphthyl)-2-propenyl bromide | HCID 22252145 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (E)-3-(4-chlorophenyl)-6-(2-naphthyl)-5-hexen-2-one | HCID 19038600 | 78% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05643958 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-397ef8e10d194d67a54872cfd2b6b3e6 |
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| 출처 메모 | uspto-grants-1997_07 |
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