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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 640362생성일: 2026년 10월 24일

Acetic Acid → 5-Fluoro-2-(3-fluoro-4-((E)-2-nitro-vinyl)phenoxymethyl)-pyridine

https://huagongshe.com/ko/reaction/640362

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물NitromethaneHCID 6375—
반응물Ammonium AcetateHCID 517165—
반응물2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehydeHCID 59255356—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물5-Fluoro-2-(3-fluoro-4-((E)-2-nitro-vinyl)phenoxymethyl)-pyridineHCID 5925507794.5%

반응 조건

온도110 °C

반응 단계

To an acetic acid (20.0 mL) solution of 2-fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)-benzaldehyde (901 mg, 3.62 mmol) described in Manufacturing Example 96-1-1 were added nitromethane (1.10 g, 18.1 mmol) and ammonium acetate (558 mg, 7.24 mmol) under nitrogen atmosphere, which was stirred for 2 hours at 110° C. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. The organic layer was 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 (1.00 g) as a crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691882B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-704e668282074e309d700a70e2b2d372
출처 메모uspto-grants-2010_04