Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1880698생성일: 2026년 10월 25일
Sodium hydride → [3-(4-Trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-on-4-yl]methyl 4-fluorobenzoate
https://huagongshe.com/reaction/1880698
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Chloromethyl 4-fluorobenzoate | HCID 11401232 | — |
| 반응물 | HCID 178517507 | HCID 178517507 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [3-(4-Trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-on-4-yl]methyl 4-fluorobenzoate | HCID 59570357 | 34.2% |
반응 단계
Into 2 ml of N,N-dimethylformamide was suspended 0.07 g of sodium hydride (60% oily), and 0.3 g of 3-(4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-one was added at room temperature. After stirring for 15 minutes, 0.29 g of chloromethyl 4-fluorobenzoate was added, and the mixture was stirred at 70° C. for 4 hours. The reaction solution was allowed to cool to room temperature, and poured into an aqueous saturated ammonium chloride solution, followed by extraction with ethyl acetate three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.17 g of [3-(4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-on-4-yl]methyl 4-fluorobenzoate (present compound (38)).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08318776B2 |
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| 출처 데이터셋 | uspto-grants-2012_11 |
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| ORD ID | ord-2ae16a5139b847cba2266c2b81f198a7 |
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| 출처 메모 | uspto-grants-2012_11 |
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