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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8113생성일: 2026년 10월 24일

Sodium hydride → 5,7-difluoro-1H-indole

https://huagongshe.com/ko/reaction/8113

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ethyl acetate hexaneHCID 21226206—
반응물ethyl N-{2,4-difluoro-6-[2-(trimethylsilyl)ethynyl]phenyl}carbamateHCID 22014809—
용매EthanolHCID 702—
생성물Sodium ethoxideHCID 2723922—
생성물5,7-difluoro-1H-indoleHCID 277873078.4%

반응 단계

Fresh sodium ethoxide is prepared by carefully adding NaH (16 g of 60% oil dispersion, 400 mmol) to 550 mL of ethanol under N2. 2-(Trimethylsilylethynyl)-4,6-difluoro-N-carbethoxyaniline (28 g, 100 mmol) in 150 mL of ethanol is added and reaction is stirred at room temperature approximately 45 minutes, while monitoring by TLC (20% ethyl acetate/hexane, UV) until all the starting material is consumed. The mixture is heated to reflux and monitored by TLC until the intermediate material is consumed (approx. 1 hour). Reaction is cooled to room temperature, concentrated, diethylether is added, washed with H2O, brine, dried (Na2SO4), filtered, concentrated, and is purified by flash chromatography (SiO2, ethyl acetate/hexane gradient) to yield 12 g of 5,7-difluoro-indole (78%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087635B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-a9d09bb02bf34689b618636a056c80b1
출처 메모uspto-grants-2006_08