참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,5-Diiodosalicylic acid | HCID 8631 | — |
| 반응물 | Phosphorus trichloride | HCID 24387 | — |
| 반응물 | 4-(1-Phenylethenyl)aniline | HCID 20040308 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Chlorobenzene | HCID 7964 | — |
| 생성물 | N-[4-(1-phenylethenyl)phenyl]-2-hydroxy-3,5-diiodobenzamide | HCID 13608340 | 43.2% |
반응 단계
To a refluxing solution of 7.9 g (0.02 mole) of 3,5-diiodosalicylic acid and 4.6 g (0.02 mole) of 1-(4-aminophenyl)-1-phenylethylene in 125 ml of chlorobenzene was added 3 g (0.022 mole) of phosphorus trichloride over a 1 hour period. The resulting mixture was refluxed for 2 hours, cooled, diluted with 100 ml of methylene chloride. The organic phase was washed with 250 ml of water and dried. The extract was evaporated to dryness. After redissolving the residue in minimum amount of methylene chloride, the solution was flash-chromatographed on a silica gel column. The desired component was eluted with 2 liters of methylene chloride/n-hexane. Evaporation of its solvent gave 4.9 g of N-[4-(1-phenylethenyl)phenyl] -2-hydroxy-3,5-diiodobenzamide. Recrystallization from aqueous ethanol gave 4.2 g of purified product, m.p. 173°-174°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04587361 |
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| 출처 데이터셋 | uspto-grants-1986_05 |
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| ORD ID | ord-9d600bc75a5743b39d2325168a77c40e |
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| 출처 메모 | uspto-grants-1986_05 |
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