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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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물Chloromethyl 4-fluorobenzoateHCID 11401232—
반응물HCID 178517507HCID 178517507—
용매DimethylformamideHCID 6228—
생성물[3-(4-Trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-on-4-yl]methyl 4-fluorobenzoateHCID 5957035734.2%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08318776B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-2ae16a5139b847cba2266c2b81f198a7
출처 메모uspto-grants-2012_11