참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Diethyl Malonate | HCID 7761 | — |
| 반응물 | 2,3,4,5-Tetrafluorobenzoyl chloride | HCID 2733689 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 생성물 | 1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioate | HCID 13564973 | 99.7% |
반응 단계
24.g of magnesium turnings are suspended in 50 ml of anhydrous ethanol. 5 ml of carbon tetrachloride are added, and, when the reaction has started, a mixture of 160 g of diethyl malonate, 100 ml of absolute ethanol and 400 ml of anhydrous toluene is added dropwise at 50°-60° C. Thereafter, the mixture is heated to 50°-60° C. for a further hour, and cooled to -5° C. to -10° C. with dry ice acetone, and a solution of 212.5 g of 2,3,4,5-tetrafluorobenzoyl chloride (1) in 80 ml of absolute toluene is slowly added dropwise at this temperature. The mixture is stirred for 1 hour at 0° to -5° C., and is allowed to reach room temperature overnight, and a mixture of 400 ml of ice water and 25 ml of concentrated sulphuric acid is allowed to run in whilst cooling with ice. The phases are separated, and extraction with toluene is repeated twice. The combined toluene solutions are washed with saturated NaCl solution and dried with Na2SO4, and the solvent is stripped off in vacuo. 335 g of diethyl 2,3,4,5-tetra-fluorobenzoylmalonate (3) are obtained as a crude product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04556658 |
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| 출처 데이터셋 | uspto-grants-1985_12 |
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| ORD ID | ord-c1be0238ed7b471b99e4c73dbf8161fe |
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| 출처 메모 | uspto-grants-1985_12 |
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