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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1760299생성일: 2026년 10월 25일

Potassium Carbonate → 5-(3-Methoxy-phenyl)-3,3-dimethyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1760299

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물(3-Methoxyphenyl)boronic acidHCID 2734370—
반응물5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-oneHCID 12052796—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
용매Ethyl AcetateHCID 8857—
생성물5-(3-Methoxy-phenyl)-3,3-dimethyl-1,3-dihydro-indol-2-oneHCID 986014131%

반응 단계

5-bromo-1,3-dihydro-3,3-dimethyl-2H-indol-2-one (0.33 g, 1.38 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.094 g) were stirred under an atmosphere of nitrogen in dimethoxyethane (12 cm3). After 15 minutes, 3-methoxyphenylboronic acid (0.42 g, 2.76 mmol) was added, followed by potassium carbonate (1.15 g, 8.34 mmol) in water (5 cm3). The reaction was heated to reflux for 5 hours, and then cooled to room temperature. Saturated aqueous ammonium chloride and EtOAc were added and the mixture was filtered. The aqueous layer was extracted with EtOAc (×2), and the combined organic layers were dried (MgSO4), filtered, and evaporated. The residue was purified by column chromatography (SiO2, EtOAc:hexane 1:3) to afford 5-(3-methoxy-phenyl)-3,3-dimethyl-1,3-dihydro-indol-2-one (0.11 g, 31%), mp=157-158° C.; 1H NMR (DMSO-d6) δ 3.34 (s, 6 H), 3.82 (s, 3 H), 6.87-6.93 (m, 2 H), 7.20-7.15 (m, 2 H), 7.37-7.32 (m, 1 H), 7.49-7.46 (m, 1 H), 7.63 (d, 1 H, J=1.14 Hz), 10.4 (s, 1 H); MS (EI) m/z 266 (M−H)−; CHN calculated for C17H17NO2: C, 76.38; H, 6.41; N, 5.24; Found: C, 76.02; H, 6.49; N, 5.02.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06841568B2
출처 데이터셋uspto-grants-2005_01
ORD IDord-b14de8c7ca4140119a43276e31c61c95
출처 메모uspto-grants-2005_01