돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240226생성일: 2026년 10월 25일

Ethyl Acetate → 2-Fluoro-N,N-dimethyl-4-(pyridin-4-yl)aniline

https://huagongshe.com/reaction/240226

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium HydroxideHCID 14797—
반응물4-(Diethylboranyl)pyridineHCID 13318871—
반응물4-bromo-2-fluoro-N,N-dimethylanilineHCID 40425364—
촉매Tetrabutylammonium BromideHCID 74236—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물2-Fluoro-N,N-dimethyl-4-(pyridin-4-yl)anilineHCID 6720218546.2%

반응 단계

4-Bromo-2-fluoro-N,N-dimethyl aniline (2.83 g, 13 mmols), tetrakis triphenyl palladium (0) (0.508 g, 0.4 mmols), diethyl (4-pyridyl borane) (1.3 g, 9 mmols), potassium hydroxide (2.81 g, 50 mmols) and tetrabutylammonium bromide (1.42 g, 4 mmols) were combined in tetrahydrofuran (50 ml). The resulting mixture was heated at reflux for 18 hrs under nitrogen then cooled to ambient temperature. Ethyl acetate (100 ml) and brine (50 ml) were added and the organic solution was separated. This was dried over magnesium sulfate filtered and evaporated to yield a yellow solid. The product was purified by column chromatography on silica eluted with ethyl acetate:hexanes 50:50 to give 0.9 g of 2-Fluoro-N,N-dimethyl-4-(pyridin-4-yl)aniline (XII) in a 44% yield as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08647827B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-679ebbcbb9de42268d302d621ffbe7de
출처 메모uspto-grants-2014_02