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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 396253생성일: 2026년 10월 24일

Potassium Carbonate → 5-(3-Chloro-4-fluoro-phenyl)-3,3-dimethyl1,3-dihydro-indol-2-one

https://huagongshe.com/ko/reaction/396253

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 2734660—
반응물5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-oneHCID 12052796—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-(3-Chloro-4-fluoro-phenyl)-3,3-dimethyl1,3-dihydro-indol-2-oneHCID 986077530%

반응 단계

A solution of 5-bromo-3,3-dimethyl-1,3-dihydro-indol-2-one (0.35 g, 1.46 mmol) and tetrakis(triphenylphosphine)palladium (0.13 g, 0.11 mmol) in dimethoxyethane (10 cm3) was stirred under N2 for 20 min. To this mixture was then added 3-chloro-4-fluorobenzene boronic acid (0.26 g, 1.49 mmol) and potassium carbonate (0.62 g, 4.5 mmol) in water (5 cm3). The solution was brought to reflux for 16 h then cooled to RT, poured into saturated ammonium chloride and extracted with EtOAc (×3). The combined organic extracts were dried (MgSO4), and evaporated. The residue was purified by column chromatography (SiO2, ethyl acetate:hexane 1:3) to afford the title compound (0.124 g, 0.43 mmol, 30%) as a white solid: m.p. 206.5-207.8° C., 1H NMR (DMSO-d6) δ 1.3 (s, 6H), 6.93 (d, J=8.1 Hz, 1H), 7.45 (dd, J=8.9, 8.9 Hz, 1H), 7.5 (dd, J=8.1, 1.8 Hz, 1H), 7.6 (ddd, J=8.9, 7.1, 2.2 Hz, 1H), 7.7 (d, J=1.8 Hz, 1H), 7.8 (dd, J=7.1, 2.2 Hz, 1H), 10.5 (s, 1H); MS (EI) m/z 289/291 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608068B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-2af50251ff384138930661acdba7f691
출처 메모uspto-grants-2003_08