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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550775생성일: 2026년 10월 24일

Sodium Iodide → 2-(2-Chloro-4-methoxyphenyl)-3-oxobutanenitrile

https://huagongshe.com/ko/reaction/550775

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물1-Bromo-2-chloro-4-methoxybenzeneHCID 2756863—
반응물Sodium t-butoxideHCID 23676156—
반응물70807-22-6HCID 71650496—
촉매TriphenylphosphineHCID 11776—
촉매palladium(II) acetateHCID 167845—
용매1,2-DimethoxyethaneHCID 8071—
용매DiglymeHCID 8150—
용매Ethyl AcetateHCID 8857—
생성물2-(2-Chloro-4-methoxyphenyl)-3-oxobutanenitrileHCID 22178154801.9%

반응 단계

Under argon gas atmosphere, to a solution of 1-bromo-2-chloro-4-methoxybenzene (120 g) in a mixed diglyme (230 mL) and 1,2-dimethoxyethane (90 mL), sodium cyano acetone (62.6 g), sodium t-butoxide (114.6 g) and sodium iodide (81.2 g) were added with stirring at room temperature to obtain a suspension. By another process, under argon gas atmosphere, a mixture of diglyme (40 mL), palladium acetate (426 mg) and triphenylphosphine (1.99 g) was stirred for about 30 minutes at 110° C. to dissolve. This solution was dropped into the above suspension. The mixture was warmed to 110 to 115° C. of internal temperature and stirred for 7 hours. The reaction mixture was cooled, diluted with ethyl acetate (480 mL) and washed with an aqueous solution of sulfuric acid (concentrated sulfuric acid 101 g/water 660 mL). The organic layer was washed with 10% saturated aqueous solution of sodium chloride (360 mL) twice. Activated charcoal (3.6 g) was added to the organic layer. The mixture was stirred for 1 hour and filtered. The filtrate was washed with ethyl acetate (240 mL) to obtain a solution of 1-cyano-1-(2-chloro-4-methoxyphenyl)propan-2-on (971.7 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947697B1
출처 데이터셋uspto-grants-2011_05
ORD IDord-81c0bcd4bf2d48be9d8504a41b7fcc44
출처 메모uspto-grants-2011_05