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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50701생성일: 2026년 10월 25일

Methyl iodide → 6-(3-Bromo-5-fluorophenyl)-1,4,4-trimethyl-1,4-dihydrobenzo[d][1,3]oxazin-2-one

https://huagongshe.com/reaction/50701

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물6-(3-Bromo-5-fluorophenyl)-4,4-dimethyl-1,4-dihydrobenzo[d][1,3]oxazin-2-oneHCID 9809875—
용매DimethylformamideHCID 6228—
생성물6-(3-Bromo-5-fluorophenyl)-1,4,4-trimethyl-1,4-dihydrobenzo[d][1,3]oxazin-2-oneHCID 1027011387%

반응 단계

To a solution of 6-(3-bromo-5-fluorophenyl)-4,4-dimethyl-1,4-dihydrobenzo[d][1,3]oxazin-2-one (0.34 g, 0.99 mmol) in dry DMF (10 mL) was added under nitrogen at room temperature sodium hydride (80 mg, 2.0 mmol) in one portion. The mixture was stirred at ambient temperature for 30 minutes, treated with iodomethane (1 mL, excess), and stirred for 2 hours. To the reaction mixture was added a cold saturated ammonium chloride solution (30 mL) and the white precipitate obtained was collected on a filter, washed with the distilled water to afford the title compound as a white solid (0.31 g, 87%): mp 157-158° C. 1H-NMR (DMSO-d6) δ 7.83 (s, 1H), 7.76 (dd, 1H, J=8.5, 2.0 Hz), 7.67 (m, 2H), 7.53 (dt, 1H, J=8.3, 1.9 Hz), 7.18 (d, 1H, J=8.5 Hz), 3.33 (s, 3H), 1.67 (s, 6H); 19F-NMR (DMSO-d6) −111.01 (m, 1F); MS (APCI) m/z 364 ([M+H]+, 96%), 366 ([M+H]+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713478B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-d23a2f6976df402baeefab153d55e184
출처 메모uspto-grants-2004_03