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HRID 32488作成日:2026年10月26日

Acetic Acid → 2-[1-(4-Nitrophenyl)ethylidene]malononitrile

https://huagongshe.com/reaction/32488

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物p-NitroacetophenoneHCID 7487—
反応物MalononitrileHCID 8010—
反応物Ammonium AcetateHCID 517165—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-[1-(4-Nitrophenyl)ethylidene]malononitrileHCID 11042086—

反応手順

p-Nitro-acetophenone (165 g/mole; 4.0 g; 24 mmoles), ammonium acetate (0.50 g) and glacial acetic acid (0.80 mL) were added to a round-bottom flask containing 20 mL toluene, and heated to reflux using a Dean-Stark trap and a reflux condenser. Separately, malononitrile (66 g/mole; 2.0 g; 30.3 mmoles) was dissolved in 5 mL dioxane and 20 mL toluene, transferred to an addition funnel and added dropwise to the heated solution of ketone. Upon completion of the addition, the system was heated for 2 hours and then cooled to room temperature. The reaction mixture was poured into 150 mL brine and 100 mL ethyl acetate. The aqueous layer was separated and washed with 50 mL ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the crude product 2-[1-(4-nitrophenyl)-ethylidene]-malononitrile (213 g/mole) was used as such in Intermediate Example 11.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427623B2
出典データセットuspto-grants-2008_09
ORD IDord-2d3178a7af6744be8777365630066edd
出典メモuspto-grants-2008_09