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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 502225생성일: 2026년 10월 25일

Iodoethane → 1-Ethyl-6-trifluoromethoxyindole-3-carbonitrile

https://huagongshe.com/reaction/502225

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Potassium CarbonateHCID 11430—
반응물Chlorosulfonyl isocyanateHCID 70918—
반응물6-(Trifluoromethoxy)-1H-indoleHCID 22048958—
용매DimethylformamideHCID 6228—
생성물1-Ethyl-6-trifluoromethoxyindole-3-carbonitrileHCID 5942583586%

반응 단계

To a solution of 6-trifluoromethoxyindole (2.68 g, 13.3 mmol) in dry DMF (10 mL) at 0° C., is added chlorosulfonylisocyanate (2.35 g, 1.44 mL, 16.6 mmol). The mixture is then brought to room temperature slowly and stirred for 1 h. The mixture is poured into ice (100 mL) and stirred for 1 h. The precipitate is collected by filtration and washed thoroughly with water and dried in vacuo, which is then dissolved in DMF (15 mL). To the solution is added K2CO3 and EtI (2.59 g, 1.34 mL, 16.6 mmol), and the mixture is stirred at 50° C. overnight. It is then poured into ice-water (200 mL). The precipitate is collected by filtration and washed with water, dried in air and purified by chromatography (silica gel, DCM) to furnish 1-ethyl-6-trifluoromethoxyindole-3-carbonitrile (2.90 g, 86%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772271B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-4793878c517a428a8120171833f08ff2
출처 메모uspto-grants-2010_08