돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32488생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/32488

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물p-NitroacetophenoneHCID 7487—
반응물MalononitrileHCID 8010—
반응물Ammonium AcetateHCID 517165—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
용매Sodium chloride; waterHCID 57417360—
생성물2-[1-(4-Nitrophenyl)ethylidene]malononitrileHCID 11042086—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427623B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-2d3178a7af6744be8777365630066edd
출처 메모uspto-grants-2008_09