Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845298생성일: 2026년 10월 26일
Pentafluoroaniline → 3-methyl-1-(2,3,4,5,6-pentafluorophenyl)-2,6-diphenyl-4(1H)-pyridinone
https://huagongshe.com/reaction/845298
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pentafluoroaniline | HCID 13040 | — |
| 반응물 | 2-Methyl-1,5-diphenylpentane-1,3,5-trione | HCID 14303545 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 3-methyl-1-(2,3,4,5,6-pentafluorophenyl)-2,6-diphenyl-4(1H)-pyridinone | HCID 14303694 | 27.7% |
반응 단계
In 110 ml of xylene were dissolved 3.1 g (0.011 mole) of 2-methyl-1,5-diphenyl-1,3,5-pentanetrione, 20.0 g (0.11 mole) of 2,3,4,5,6-pentafluoroaniline, 3.1 g (0.016 mole) of paratoluenesulfonic acid and 22.0 g of Molecular Sieves 5A, followed by reflux for 1 hours. After cooling the reaction mixture, solid matter was removed by filtration and the filtrate was then concentrated. After 200 ml of chloroform was added, the resultant solution in chloroform was washed first with 50 ml of 10% hydrochloric acid and then with 50 ml of a 10% aqueous solution of sodium hydroxide. After washing the solution in chloroform further with water, it was dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate, the solvent was distilled off and the residue was subjected to column chromatography (eluent: 50:1 mixed solvent of chloroform and methanol). The resulting crystals were recrystallized from a 1:1 mixed solvent of acetone and hexane, thereby affording 1.3 g of 3-methyl-1-(2,3,4,5,6-pentafluorophenyl)-2,6-diphenyl-4(1H)-pyridinone having a melting point of 192°-194° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04757081 |
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| 출처 데이터셋 | uspto-grants-1988_07 |
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| ORD ID | ord-4ef7abd484324b428735bd7ac7cba367 |
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| 출처 메모 | uspto-grants-1988_07 |
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