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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51399생성일: 2026년 10월 24일

o-Xylyl bromide → 9-[(2-methylphenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one

https://huagongshe.com/ko/reaction/51399

반응식

참여 물질

역할이름HCID투입량
반응물o-Xylyl bromideHCID 6992—
반응물Potassium CarbonateHCID 11430—
반응물methyl 4-oxo-2,3,4,9-tetrahydro-1H-carbazole-5-carboxylateHCID 11368514—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물9-[(2-methylphenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-oneHCID 2273903898%

반응 단계

A suspension of 5-carbomethoxy-1,2-dihydro-9H-carbazol-4(3H)-one (870 mg, 3.58 mM), a-bromo-o-xylene (662 mg, 3.58 mM), and potassium carbonate (500 mg, 3.61 mM) in 20 mL DMF was stirred at room temperature for 20 hours. The mixture was diluted with ethyl acetate, washed with H2O and saturated brine, dried over anhydrous magnesium sulfate, filtered, concentrated to afford 1.21 g (98%) of the 9-[(2-methylphenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one as a dark oil. 1H NMR (DMSO-d6) δ7.5-7.2 (m, 4H), 7.15 (t, 1H, J=8 Hz), 7.0 (t, 1H, J=8 Hz), 6.15 (d, 1H, J=8 Hz), 5.55 (s, 2H), 3.85 (s, 3H), 2.6 (m, 2H), 2.4 (m, 2H), 2.4 (s, 3H), and 2.1 (m, 2H). IR (CHCl3, cm−1) 3010, 2952, 1724, 1671, 1653, 1604, 1460, 1444, 1290, 1174, and 1122. MS (ES) m/e 348.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713645B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-baad6309beef405695969d0d0b60acdb
출처 메모uspto-grants-2004_03