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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2177002생성일: 2026년 10월 24일

Ethyl Acetate → 2-Fluoro-6-(2,3,5-trifluorobenzyloxy)-benzonitrile

https://huagongshe.com/ko/reaction/2177002

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물2,6-DifluorobenzonitrileHCID 74695—
반응물2,3,5-Trifluorobenzyl alcoholHCID 2777030—
용매DimethylformamideHCID 6228—
생성물2-Fluoro-6-(2,3,5-trifluorobenzyloxy)-benzonitrileHCID 6692422672.9%

반응 단계

To a cold (ice water) suspension of sodium hydride (407 mg; 10 mmol) in anhydrous DMF (4 is added a solution of 2,3,5-trifluorobenzyl alcohol (1.62 g; 10 mmol) in anhydrous DMF (5 mL) over 10 minutes. After allowing to room temperature over 1 hour, this solution is added to a cold (ice water) stirred solution of 2,6-difluorobenzonitrile (1.56 gm; 11 mmol) in anhydrous DMF (5 mL), and allowed to room temperature over 3 hours. TLC (25% EA/Hex) was incomplete so the reaction was continued at room temperature for an additional 2 hours. The reaction mixture is poured into ice water with vigorous stirring and the resulting solid is filtered, washed with water, and dried under vacuum at 40° C. for 4.5 hours to give 2.05 grams of 2-fluoro-6-(2,3,5-trifluorobenzyloxy)-benzonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09067897B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-d20ea2a180c9470d9b6942ac3c970e66
출처 메모uspto-grants-2015_06