戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 550775作成日:2026年10月25日

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

https://huagongshe.com/reaction/550775

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物1-Bromo-2-chloro-4-methoxybenzeneHCID 2756863—
反応物Sodium t-butoxideHCID 23676156—
反応物70807-22-6HCID 71650496—
触媒TriphenylphosphineHCID 11776—
触媒palladium(II) acetateHCID 167845—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒DiglymeHCID 8150—
溶媒Ethyl AcetateHCID 8857—
生成物2-(2-Chloro-4-methoxyphenyl)-3-oxobutanenitrileHCID 22178154801.9%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947697B1
出典データセットuspto-grants-2011_05
ORD IDord-81c0bcd4bf2d48be9d8504a41b7fcc44
出典メモuspto-grants-2011_05