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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226947생성일: 2026년 10월 25일

m-Xylyl bromide → 3-(3-Methyl-benzoyl)-1-(3-methyl-benzyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/226947

반응식

참여 물질

역할이름HCID투입량
반응물m-Xylyl bromideHCID 12099—
반응물Sodium hydrideHCID 24758—
반응물3-(3-methyl-benzoyl)-2,3-dihydro-1H-quinolin-4-oneHCID 67071952—
용매DimethylformamideHCID 6228—
생성물3-(3-Methyl-benzoyl)-1-(3-methyl-benzyl)-1H-quinolin-4-oneHCID 1673085350.1%

반응 단계

Compound 4y was prepared following the procedure outlined in Step 3 of Example 1 using 26 mg (0.65 mmol) of sodium hydride (60%), 132 mg (0.50 mmol) of 3-(3-methyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one, 3 mL of anhydrous dimethylformamide, and 120 mg (0.65 mmol) of 3-methylbenzylbromide. The crude product was purified by flash chromatography to yield 92 mg of a colorless solid 4y: LC-MSD, m/z for C25H21NO2, [M+H]+=368.5, [M+2H]+=369.5; Reverse phase HPLC (gradient acetonitrile 0.1% TFA 20-95% in 4 min) retention time=2.586 min; 1H NMR (400 MHz, CDCl3/HCl): δ 2.37 (s, 3H), 2.42 (s, 3H), 5.39 (s, 2H), 7.01 (d, 2H), 7.15 (d, 1H), 7.22-7.44 (m, 5H), 7.55-7.58 (m, 3H), 8.29 (s, 1H), 8.47 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557213B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-90fef07af96448c2948cb4a7c9a94fe4
출처 메모uspto-grants-2009_07