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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 402844생성일: 2026년 10월 25일

Potassium Carbonate → 1-(propan-2-yl)-4-(2,3,4-trifluorophenyl)-1H-indole-3-carboxaldehyde

https://huagongshe.com/reaction/402844

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,3,4-Trifluorobenzeneboronic acidHCID 2783280—
반응물4-bromo-1-isopropyl-1H-indole-3-carbaldehydeHCID 77230881—
촉매HCID 178454869HCID 178454869—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물1-(propan-2-yl)-4-(2,3,4-trifluorophenyl)-1H-indole-3-carboxaldehydeHCID 8668528168.7%

반응 조건

온도140 °C

반응 단계

To a solution of 4-bromo-1-(propan-2-yl)-1H-indole-3-carboxaldehyde (100 mg, 0.376 mmol) and 2,3,4-trifluorophenylboronic acid (79 mg, 0.451 mmol) in dioxane (2 mL) and water (0.5 mL) in a 5 mL microwave reaction vial was added potassium carbonate (156 mg, 1.13 mmol) and dichloro[1,1′-bis(di-t-butylphosphino)ferrocene]palladium (II) (25 mg, 0.038 mmol). The reaction was placed under nitrogen, sealed and heated in a microwave reactor at 140° C. for 15 minutes. The solvent was removed in vacuo and the residue was partitioned with ethyl acetate and aqueous sodium bicarbonate and extracted twice with ethyl acetate. The organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified on silica gel (COMBI FLASH 24 gm column, gradient of 0-100% ethyl acetate/hexanes) to give the title intermediate (82 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08742110B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-32e07e7475ba49d9b3530fab92a58071
출처 메모uspto-grants-2014_06