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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 915184생성일: 2026년 10월 27일

Water → 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one

https://huagongshe.com/reaction/915184

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물IodoethaneHCID 6340—
반응물Potassium HydroxideHCID 14797—
반응물7-Bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-oneHCID 21966423—
용매Dimethyl SulfoxideHCID 679—
생성물7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-oneHCID 21966429104.5%

반응 조건

온도0 °C

반응 단계

A mixture of powdered potassium hydroxide (3.35 g, 59.67 mmol) in DMSO (40 mL) was stirred at 0° C. for 10 min. 7-bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one (Example 2c) (8.0 g, 29.83 mmol) was added cautiously, followed immediately by the addition of ethyl iodide (12 mL, 149.17 mmol). The reaction mixture was kept at 0° C. for 30 min then slowly warmed up to room temperature and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with dichloromethane washed with water and brine, dried (Mg2SO4), filtered and evaporated to give 8.8 g of 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one and used without further purification in the Suzuki coupling (step a). 1H NMR (300 MHz; CDCl3): 1.24 (t, J=7.2 Hz, 1 H), 1.25 (s, 6 H), 2.37 (s, 3 H), 2.45 (s, 2 H), 3.98 (q, 2 H), 7.13 (s, 1 H), 7.18 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265139B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-2409a829d379468393ded1b92a9a238c
출처 메모uspto-grants-2007_09