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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1797409생성일: 2026년 10월 25일

N-bromobutanimide → 2-(4-Methoxy-2-methylphenyl)acetonitrile

https://huagongshe.com/reaction/1797409

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물3,4-DimethylanisoleHCID 78411—
촉매AzobisisobutyronitrileHCID 6547—
용매Carbon TetrachlorideHCID 5943—
생성물2-(4-Methoxy-2-methylphenyl)acetonitrileHCID 380102473.2%

반응 단계

Under argon atmosphere, a mixture of N-bromosuccinimide (17.8 g) and 2,2′-azobisisobutyronitrile (492 mg) was added to a solution of 1,2-dimethyl-4-methoxybenzene (13.6 g) in carbon tetrachloride (200 ml). The mixture was refluxed for 6.5 hours. The reaction mixture was cooled with ice-bath. An insoluble matter was removed by filtration, and washed with carbon tetrachloride. A combined filtrate was concentrated. The residue was dissolved into N,N-dimethylformamide (100 ml) and sodium cyanide (9.86 g) was added to the mixture. The mixture was stirred over night at room temperature. The reaction mixture was poured into water, and the mixture was extracted with diethyl ether. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:n-hexane=1:6→1:4) to give the title compound (11.78 g) having the following physical data.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07034153B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-c96fe42e0c944e75a11f6a14134c737f
출처 메모uspto-grants-2006_04