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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1881034생성일: 2026년 10월 27일

Aniline → N-2-Pyridylaniline

https://huagongshe.com/reaction/1881034

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참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물2-BromopyridineHCID 7973—
반응물Ethyl AcetateHCID 8857—
반응물Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물N-2-PyridylanilineHCID 8113072%

반응 조건

온도80 °C

반응 단계

2-bromopyridine (3.0 g) and aniline (5.3 g) were dissolved in toluene (40 mL), tris(dibenzylideneacetone)dipalladium (0) (350 mg), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (480 mg) and sodium tert-butoxide (2.6 g) were added, then stirred at 80° C. for three hours. Ethyl acetate (100 mL) was added to the reaction solution, and then washed with water (100 mL). The organic layer was extracted with 2N hydrochloric acid (100 mL), and washed with ethyl acetate (100 mL). The water layer was made alkaline with 2N sodium hydroxide aqueous solution (150 mL) and then extracted with ethyl acetate (200 mL). The organic layer was washed with a saturated sodium chloride solution (50 mL). After drying on anhydrous sodium sulfate, filtration and vacuum concentration, the residue was washed with diethyl ether to give the above-identified compound (2.1 g, yield 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08318781B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-0283c671889d4ec381d80ea07ab0abc3
출처 메모uspto-grants-2012_11