Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48078생성일: 2026년 10월 24일
Triethylamine → 2,2,2-Trifluoro-1-[[(3-fluoro-phenyl)[3-(trifluoromethyl)benzoyl]amino]methyl]ethyl 3-trifluoromethyl-benzoate
https://huagongshe.com/ko/reaction/48078
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-(Trifluoromethyl)benzoyl chloride | HCID 75257 | — |
| 반응물 | 3-[(3-Fluorophenyl)amino]-1,1,1-trifluoro-2-propanol | HCID 11138733 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 2,2,2-Trifluoro-1-[[(3-fluoro-phenyl)[3-(trifluoromethyl)benzoyl]amino]methyl]ethyl 3-trifluoromethyl-benzoate | HCID 10951914 | 73.3% |
반응 단계
The 3-[(3-fluorophenyl)amino]-1,1,1-trifluoro-2-propanol (446 mg, 2.0 mmol) from EX-662A and triethylamine (544 mg) were dissolved in anhydrous CHCl3 (30 mL) and cooled to 0° C. Then a solution of 3-trifluoromethylbenzoyl chloride (1.04 g, 5.0 mmol) in anhydrous CHCl3 (6 mL) was added over a period of 15 min. The solution was stirred at room temperature. After 14 h, the solution was washed with 5% NaHCO3 (2×20 mL) and brine (2×10 mL), and then dried over anhydrous MgSO4. Removal of the solvent in vacuo gave 832 mg (73%) of the desired 2,2,2-trifluoro-1-[[(3-fluoro-phenyl)[3-(trifluoromethyl)benzoyl]amino]methyl]ethyl 3-trifluoromethyl-benzoate product as an amber oil, which was greater than 95% pure by reverse phase HPLC analysis. 1H NMR (CDCl3) δ7.25-8.39 (m, 9H), 7.02 (q, 1H), 6.71 (m, 2H), 6.11 (m, 1H), 4.58 (dd, 1H), 4.35 (dd, 1H). 19F NMR (CDCl3) δ−64.4 (m, 6F), −77.4 (s, 3F), −111.3 (m, 1F). HRMS calcd. for C25H15F10NO3: 568.0970 [M+H]+, found: 568.0968.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699898B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-c74cdf4c5ca84d5e928b959b06210e26 |
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| 출처 메모 | uspto-grants-2004_03 |
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