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HRID 1792859作成日:2026年10月26日

4-Cyanobenzaldehyde → (E)-4-[3-Acetyl-1-(3,5-dichlorophenyl)-2,5-dioxoimidazolidin-4-ylidenemethyl]benzonitrile

https://huagongshe.com/reaction/1792859

反応式

関与物質

役割名称HCID仕込み量
反応物4-CyanobenzaldehydeHCID 66042—
反応物Sodium AcetateHCID 517045—
反応物3-(3,5-Dichlorophenyl)-2,4-dioxoimidazolidine-1-carboxylic acid tert-butyl esterHCID 23588558—
溶媒Acetic AnhydrideHCID 7918—
生成物(E)-4-[3-Acetyl-1-(3,5-dichlorophenyl)-2,5-dioxoimidazolidin-4-ylidenemethyl]benzonitrileHCID 10111572109.9%

反応手順

A mixture of 3-(3,5-dichlorophenyl)-2,4-dioxoimidazolidine-1-carboxylic acid tert-butyl ester (3.45 g, 10 mmol) (Preparation 11), 4-cyanobenzaldehyde (1.31 g, 10 mmol) and NaOAc (0.82 g, 10 mmol) was refluxed for 3 h in Ac2O (50 ml). The solid obtained after concentration was taken into a mixture of ice/water and DCM. The organic layer was dried and concentrated to yield a solid (4.4 g) which was chromatographed over silica gel (eluent: DCM) to yield 4-[3-acetyl-1-(3,5-dichlorophenyl)-2,5-dioxoimidazolidin-4-ylidenemethyl]-benzonitrile as a white solid (1.25 g). mp=212° C. 1H NMR (CDCl3): 8.52 (1H, s), 7.6–7.75 (4H, m), 7.43 (1H, m), 7.37 (2H, m), 2.78 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07078420B2
出典データセットuspto-grants-2006_07
ORD IDord-c24b3f2993e946fcbda0dfb1310bbbb5
出典メモuspto-grants-2006_07