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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338219생성일: 2026년 10월 25일

Potassium Carbonate → 6-Chloro-5-(4-hydroxymethyl-phenyl)-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/338219

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
반응물5-bromo-6-chloro-1H-indole-3-carbaldehydeHCID 86698566—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
용매Ethylacetate heptaneHCID 21899848—
생성물6-Chloro-5-(4-hydroxymethyl-phenyl)-1H-indole-3-carbaldehydeHCID 8669857020%

반응 조건

온도120 °C

반응 단계

A mixture of 5-bromo-6-chloro-1H-indole-3-carbaldehyde (783 mg, 3.03 mmol), 4-(hydroxymethyl)benzene boronic acid (460 mg, 3.03 mmol), 2N aqueous potassium carbonate (6.4 mL, 13 mmol) in toluene (9 mL) and EtOH (13 mL) was degassed with N2 for 5 minutes, then treated with [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (247 mg, 0.30 mmol). The mixture was heated in a sealed tube to 120° C. and stirred for 2.5 hours. The reaction mixture was cooled to room temperature, diluted with EtOAc (200 mL), then washed with water (50 mL) and brine (50 mL). The organic layer was dried over MgSO4 and concentrated in vacuo. The resulting brown foam was purified by flash chromatography (20-100% EtOAc/heptane) to afford a pale yellow solid. The solid was dissolved in 5:1 EtOAc/heptane (30 mL), and a colorless precipitate formed. The precipitate was collected by filtration, washed with heptane and dried under vacuum to afford the title compound (173 mg, 20% yield) as a colorless solid. MS (ES+) 286.0 (M+H)+. 1H NMR (500 MHz, CD3OD) δ 9.92 (s, 1H) 8.07 (s, 1H) 8.25 (s, 1H) 7.64 (s, 1H) 7.44 (m, 4H) 4.70 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889730B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-f76aa54d9f294fed941559c9d9058359
출처 메모uspto-grants-2014_11