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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78287생성일: 2026년 10월 24일

Acetic Acid → 2-Benzyloxy-5-(2-nitro-ethyl)pyridine

https://huagongshe.com/ko/reaction/78287

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물WaterHCID 962—
반응물VertellusHCID 22959485—
반응물2-(Benzyloxy)-5-[(E)-2-nitroethenyl]pyridineHCID 56605146—
용매Dimethyl SulfoxideHCID 679—
생성물2-Benzyloxy-5-(2-nitro-ethyl)pyridineHCID 5925506940.7%

반응 단계

To a solution of 2-benzyloxy-5-((E)-2-nitro-vinyl)-pyridine described in Manufacturing Example 231-1-3 (44.0 g, 172 mmol) and acetic acid (44.0 mL) in dimethyl sulfoxide (200 mL) was added sodium borohydrate (11.0 g, 275 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 30 minutes. Water was added to this reaction solution at room temperature while cooling appropriately, which was then partitioned into water and ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (18.1 g, 40.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-a18c599c3461453e87d6688ff1090134
출처 메모uspto-grants-2014_09