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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17355생성일: 2026년 10월 24일

Water → 7-Fluoro-2-(2-methoxy-1,1-dimethylethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/ko/reaction/17355

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Tetrafluoroboric acidHCID 28118—
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물7-Fluoro-2-(2-hydroxy-1,1-dimethylethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 68585957—
용매DichloromethaneHCID 6344—
생성물7-Fluoro-2-(2-methoxy-1,1-dimethylethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 6858553179%

반응 조건

온도0 °C

반응 단계

7-Fluoro-2-(2-hydroxy-1,1-dimethylethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile (I-99) (50 mg, 0.15 mmol) was dissolved in methylene chloride (0.5 ml), aqueous 42% tetrafluoroboric acid solution (32 μl, 0.15 mmol) was added, then with cooling with ice, trimethylsilyldiazomethane (2 M hexane solution, 77 μl, 0.15 mmol) was dropwise added, followed by stirring at 0° C. for 10 minutes, further trimethylsilyldiazomethane (2 M, hexane solution, 77 μl, 0.15 mmol) was dropwise added, followed by stirring at 0° C. for 1 hour. After the reaction, water was added followed by extraction with methylene and washing with saturated brine. The obtained organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated away under reduced pressure. The resulting residue was subjected to preparative thin-layer silica gel column chromatography, eluted with n-hexane/ethyl acetate (5:1, v/v) to obtain the entitled compound (41.2 mg, 79%) as a colorless transparent oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7ca364c2b9624ab2a5b8c527332b1845
출처 메모uspto-grants-2010_06