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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77898생성일: 2026년 10월 24일

Acetic Acid → 4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine

https://huagongshe.com/ko/reaction/77898

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물NitromethaneHCID 6375—
반응물Ammonium AcetateHCID 517165—
반응물4-(4-Methyl-pyridin-2-yloxymethyl)-benzaldehydeHCID 59255467—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridineHCID 59255134109.4%

반응 조건

온도100 °C

반응 단계

To an acetic acid (20.0 mL) solution of 4-(4-methyl-pyridin-2-yloxymethyl)-benzaldehyde (2.60 g, 11.5 mmol) described in Manufacturing Example 43-1-2 were added nitromethane (3.50 g, 57.3 mmol) and ammonium acetate (1.76 g, 22.9 mmol) at room temperature under nitrogen atmosphere, which was stirred for 4 hours at 100° C. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (3.40 g) as a crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-cc6dd927238f4dbab11b01f4a7bf78c3
출처 메모uspto-grants-2014_09