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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,3,4-Trifluorobenzeneboronic acid | HCID 2783280 | — |
| 반응물 | 4-bromo-1-isopropyl-1H-indole-3-carbaldehyde | HCID 77230881 | — |
| 촉매 | HCID 178454869 | HCID 178454869 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 1-(propan-2-yl)-4-(2,3,4-trifluorophenyl)-1H-indole-3-carboxaldehyde | HCID 86685281 | 68.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08742110B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-32e07e7475ba49d9b3530fab92a58071 |
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| 출처 메모 | uspto-grants-2014_06 |
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