참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 반응물 | Ethylmalonic acid | HCID 11756 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ethylpropanedioate | HCID 6950106 | — |
| 반응물 | Dipyranyl ethylmalonate | HCID 19976934 | — |
| 반응물 | 3-(4-Methylphenyl)isoxazole-5-carboxylic acid chloride | HCID 53715915 | — |
| 반응물 | Sodium dipyranyl malonate | HCID 67715643 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(4-Methylphenyl)-5-butyrylisoxazole | HCID 19976953 | — |
반응 단계
In 50 ml of benzene, 2.6 g (57.5 mmol) of 60% sodium hydride were added to dipyranyl ethylmalonate which had been prepared from 5.7 g (43.2 mmol) of ethylmalonic acid, 9.0 g (107.1 mmol) of 3,4-dihydropyran and 1 droplet of concentrated sulfuric acid. At 40°-50° C., the ethylmalonate was converted to sodium dipyranyl malonate, to which a tetrahydrofuran solution of 3-(4-methylphenyl)isoxazole-5-carboxylic acid chloride synthesized above in the procedure (3) was added dropwise at room temperature. They were reacted for 3 hours. The reaction mixture was added with 10 ml of acetic acid and then heated under reflux for 6 hours. The mixture thus obtained was added into water and then extracted with benzene. The benzene extract was washed successively with an aqueous solution of sodium hydrogencarbonate and water. The organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off. Hexane was added to the residue, and 3-(4-methylphenyl)-5-butyrylisoxazole precipitated as crystals was collected by filtration.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05498619 |
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| 출처 데이터셋 | uspto-grants-1996_03 |
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| ORD ID | ord-373eee14e52f4e4fbf79c7abb5aecdde |
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| 출처 메모 | uspto-grants-1996_03 |
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