돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489921생성일: 2026년 10월 24일

Piperidine → 4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-one

https://huagongshe.com/ko/reaction/489921

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물3-Fluoro-p-anisaldehydeHCID 67696—
반응물4-PyridinylacetoneHCID 80552—
용매TolueneHCID 1140—
생성물4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-oneHCID 69373148393.2%

반응 단계

A solution of 4-pyridylacetone (1.0 g, 7.4 mmol), 3-fluoro-p-anisaldehyde (1.25 g, 8.1 mmol), and piperidine (0.13 g, 1.5 mmol) in toluene (50 ml) was heated to reflux. After 18 hours, the reaction was cooled to room temperature and the solvent was removed under reduced pressure. The crude product (3.0 g) was purified by column chromatography (silica gel, 65:35 ethyl acetate/hexane) to give 4-(3-fluoro-4-methoxylphenyl) -3-pyridyl-3-butene-2-one as a pale yellow solid (1.60 g, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06979686B1
출처 데이터셋uspto-grants-2005_12
ORD IDord-f9ced75ef53c4362afa8e12efbbe0011
출처 메모uspto-grants-2005_12