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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2079892생성일: 2026년 10월 25일

Sodium Bicarbonate → 4-(6-nitro-1H-indol-3-yl)-benzonitrile

https://huagongshe.com/reaction/2079892

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물4-(1-benzenesulfonyl-6-nitro-1H-indol-3-yl)-benzonitrileHCID 57442242—
용매AcetoneHCID 180—
용매TetrahydrofuranHCID 8028—
생성물4-(6-nitro-1H-indol-3-yl)-benzonitrileHCID 57442197—

반응 단계

Add 100 mL of 1 M TBAF in THF to a slurry of 4-(1-benzenesulfonyl-6-nitro-1H-indol-3-yl)-benzonitrile 8 (14.3 g, 35 mmol) in 50 mL of THF. Monitor the reaction by TLC. If starting material remains add more 1 M TBAF in THF until the reaction is complete. Pour reaction mixture into 200 mL of saturated aqueous sodium bicarbonate and then extract the resulting solution 3× with EtOAc. Combine the organic extracts and wash the extracts with saturated aqueous bicarbonate, water (2×), brine. Dry the resulting organic solution over Na2SO4, filter, and then remove the organic solvent to provide a solid. Redisolve the solid in ˜400 mL of acetone with heating and then add ˜100 mL hexanes until a precipitate forms. Let the solution cool and then collect the precipitate. Concentrate the filtrates and redisolve in ˜300 mL of 50% acetone/hexanes with heating. Let the solution cool and then place in a freezer at −20° C. overnight. Collect the crystals that form. The combined yield of the title compound is 6.71 g, 25.5 mmol, 72%. LRMS (API ES−)=262.0 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07932284B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-57336213eff141c2b05476d1b1da5eae
출처 메모uspto-grants-2011_04