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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227604생성일: 2026년 10월 23일

p-Nitroacetophenone → (2E)-1-(4-nitrophenyl)-3-pyridin-4-ylprop-2-en-1-one

https://huagongshe.com/ko/reaction/227604

반응식

참여 물질

역할이름HCID투입량
반응물p-NitroacetophenoneHCID 7487—
반응물4-PyridinecarboxaldehydeHCID 13389—
반응물Sodium HydroxideHCID 14798—
용매WaterHCID 962—
용매Water ethanolHCID 19096565—
생성물(2E)-1-(4-nitrophenyl)-3-pyridin-4-ylprop-2-en-1-oneHCID 608819725.3%

반응 단계

A suspension of 4′-nitroacetophenone (5 g, 30.3 mmol) and 4-pyridinecarboxaldehyde (2.89 mL, 30.3 mmol) in water (45 mL) at room temperature was treated with 6% NaOH in H2O/ethanol (2:1)(0.606 mL), stirred overnight, and filtered. The filter cake was washed with water and small amount of ethanol then triturated with dichloromethane to provide 1.95 g (25%) of the desired product. MS(ESI(+)) m/e 255 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560552B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-66be6540069849619d3c20efa2b68ca7
출처 메모uspto-grants-2009_07