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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9329생성일: 2026년 10월 25일

Potassium Carbonate → 5-(3-Chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/9329

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물(3-Chlorophenyl)boronic acidHCID 2734323—
반응물5-Bromo-3,3-diethyl-1,3-dihydro-2H-indol-2-oneHCID 21986250—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-(3-Chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-oneHCID 994824627%

반응 단계

A solution of 5-bromo-1,3-dihydro-3,3-diethyl-[2H]-indol-2-one (2.7 g, 10 mmol), 3-chlorophenylboronic acid (1.6 g, 10 mmol), potassium carbonate (4 g, 30 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.5 g, 0.4 mmol) in dimethoxyethane (100 ml), ethanol (25 ml), and water (25 ml) was heated to reflux for 6 hours. After cooling to room temperature, the mixture was diluted with water and extracted with EtOAc (2×). The combined organic extracts were washed with water, then brine, dried (MgSO4) and evaporated. The residue was purified by column chromatography (SiO2, EtOAc:hexane 1:3) to afford 5-(3-chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-one compound (0.8 g, 27%), m.p. 195–197° C.; 1H-NMR (DMSO-d6) δ 7.70 (t, 1H, J=2 Hz), 7.62–7.60 (m, 1H), 7.58 (d, 1H, J=1.7 Hz), 7.52 (dd, 1H, J=8.1, 2 Hz), 7.43 (t, 1H, J=7.9 Hz), 7.36–7.33 (m, 1H), 6.90 (d, 1H, J=8.1 Hz), 1.87–1.70 (m, 4H) and 0.52 (t, 6H, J=7.4 Hz); MS (+)APCI) m/z 300/302 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091234B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6ee58afad1c54d4ca431da562fb42f20
출처 메모uspto-grants-2006_08