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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 661884생성일: 2026년 10월 27일

Potassium Carbonate → 2-(3-bromo-2-methylphenyl)-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/reaction/661884

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,6-DibromotolueneHCID 34681—
반응물3,4-dihydroisoquinolin-1(2H)-oneHCID 150896—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
용매DichloromethaneHCID 6344—
생성물2-(3-bromo-2-methylphenyl)-3,4-dihydroisoquinolin-1(2H)-oneHCID 5937511466.1%

반응 조건

온도150 °C

반응 단계

Step 2 A mixture of 1,3-dibromo-2-methylbenzene (340 mg, 1.359 mmol), 3,4-dihydroisoquinolin-1(2H)-one (100 mg, 0.679 mmol) and potassium carbonate (94 mg, 0.679 mmol) in DMSO (2 mL) was purged with nitrogen, treated with copper (I) iodide (25.9 mg, 0.136 mmol) and heated at 150° C. for 3.5 h. The mixture was combined with that from a second reaction using 1,3-dibromo-2-methylbenzene (2.59 g, 10.36 mmol) and 3,4-dihydroisoquinolin-1(2H)-one (508 mg, 3.45 mmol), diluted with DCM and filtered through Celite. The filtrate was washed with 5% aqueous ammonium hydroxide, dried and concentrated. The residue was purified by column chromatography (eluting with hexane-EtOAc) to provide 2-(3-bromo-2-methylphenyl)-3,4-dihydroisoquinolin-1(2H)-one as a yellow solid (142 mg, 11%). 1H NMR (400 MHz, chloroform-d) δ 8.15 (1H, dd, J=7.70, 1.10 Hz), 7.55 (1H, dd, J=7.92, 1.10 Hz), 7.46-7.51 (1H, m), 7.37-7.42 (1H, m), 7.24-7.28 (1H, m), 7.17-7.21 (1H, m), 7.09-7.16 (1H, m), 3.95 (1H, ddd, J=12.21, 10.12, 4.73 Hz), 3.73 (1 H, ddd, J=11.94, 6.33, 5.28 Hz), 3.26 (1H, ddd, J=15.74, 10.23, 5.28 Hz), 3.06-3.14 (1H, m), 2.36 (3H, s). Mass spectrum m/z 316, 318 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084620B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-98e0e8da894c45a68096c12098af0b37
출처 메모uspto-grants-2011_12