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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1023166생성일: 2026년 10월 27일

Sodium hydride → 6-bromo-1-(4-methoxybenzyl)quinolin-2(1H)-one

https://huagongshe.com/reaction/1023166

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Methyloxybenzyl chlorideHCID 69993—
반응물6-Bromoquinolin-2(1H)-oneHCID 12378943—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물6-bromo-1-(4-methoxybenzyl)quinolin-2(1H)-oneHCID 6727208280%

반응 단계

To a stirred solution of 6-bromoquinolin-2(1H)-one (2 g, 8.92 mmol) in DMF (20 mL) was added NaH (0.26 g, 10.7 mmol) at 0° C. After stirring for 30 min, 1-(chloromethyl)-4-methoxybenzene (1.67 g, 10.7 mmol) was added and the resulting reaction mixture was stirred at RT overnight. The reaction mixture was diluted with water and the precipitate was filtered, washed with water and dried. The crude product was purified by flash chromatography on silica gel using hexane/ethyl acetate to give 6-bromo-1-(4-methoxybenzyl)quinolin-2(1H)-one as yellow solid (2.4 g, 80%). 1HNMR: 400 MHz, DMSO-d6: δ 3.70 (s, 3H), 5.43 (s, 2H), 6.78 (d, J=9.60 Hz, 1H), 6.87 (dd, J=2.00, 6.40 Hz, 2H), 7.14 (d, J=8.80 Hz, 2H), 7.38 (d, J=8.80 Hz, 1H), 7.66 (dd, J=2.40, 8.80 Hz, 1H), 7.94 (d, J=−8.40 Hz, 1H), 8.01 (d, J=2.40 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722670B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-992b80b66c134eafa232b5455bad1807
출처 메모uspto-grants-2014_05