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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1691054생성일: 2026년 10월 25일

Nitromethane → 2-(3-((E)-2-nitro-vinyl)-phenoxymethyl)-pyridine

https://huagongshe.com/reaction/1691054

반응식

참여 물질

역할이름HCID투입량
반응물NitromethaneHCID 6375—
반응물Ammonium AcetateHCID 517165—
반응물3-(Pyridin-2-ylmethoxy)benzaldehydeHCID 6483805—
용매Acetic AcidHCID 176—
생성물2-(3-((E)-2-nitro-vinyl)-phenoxymethyl)-pyridineHCID 5925524971.4%

반응 조건

온도100 °C

반응 단계

A mixture of 3-(pyridin-2-ylmethoxy)-benzaldehyde (2.98 g, 14 mmol) described in Manufacturing Example 60-1-1, nitromethane (1.51 mL, 28 mmol), ammonium acetate (1.62 g, 21 mmol) and acetic acid (30 mL) was stirred for 6 hours at 100° C. This mixture was cooled to room temperature, concentrated under a reduced pressure, and diluted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=4:1-2:1-1:1) to obtain the title compound (2.56 g, 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153662B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-b6b7bcf0b05c41598e0562e71c1a0410
출처 메모uspto-grants-2012_04