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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55967생성일: 2026년 10월 25일

4-Fluorobenzonitrile → 2-[2-(4-Cyano-phenoxy)-1-hydroxy-1-methyl-ethyl]-6-trifluoromethyl-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/55967

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorobenzonitrileHCID 14517—
반응물Sodium hydrideHCID 24758—
반응물2-(1,2-Dihydroxy-1-methyl-ethyl)-6-trifluoromethyl-1H-indole-5-carbonitrileHCID 66864495—
용매DimethylformamideHCID 6228—
생성물2-[2-(4-Cyano-phenoxy)-1-hydroxy-1-methyl-ethyl]-6-trifluoromethyl-1H-indole-5-carbonitrileHCID 66865341—

반응 단계

To a solution of 2-(1,2-dihydroxy-1-methyl-ethyl)-6-trifluoromethyl-1-H-indole-5-carbonitrile (209.6 mg, 0.7374 mmol) in dry DMF (4 ml) was added NaH (60 mg, 1.4749 mmol, 60% in mineral oil). After the reaction mixture was stirred at room temperature for 30 min., 4-fluorobenzonitrile (98.15 mg, 0.8115 mmol) was added, and the reaction mixture stirred at room temperature. After HPLC indicated the consumption of starting material, the reaction mixture was poured onto water and extracted with ethyl acetate. The organic layer was washed with 10% LiCl, brine and dried over MgSO4. Column chromatography (EtOAc/Hexanes 50%-100%) yielded the title product as a light yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434688B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-51b0b972ad60497995c3121fa100981b
출처 메모uspto-grants-2016_09