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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572생성일: 2026년 10월 23일

Aniline → N-phenylpyridin-4-amine

https://huagongshe.com/ko/reaction/572

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참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물4-BromopyridineHCID 14268—
시약Sodium t-butoxideHCID 23676156—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Palladium (II) acetateHCID 4144353—
용매TolueneHCID 1140—
생성물N-phenylpyridin-4-amineHCID 8994540.92%

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온도100 °C

반응 단계

ANILINE (1.730 mL, 18.99 mmol) was added to 4-bromopyridine (2.5 g, 15.82 mmol), PALLADIUM(II) ACETATE (0.071 g, 0.32 mmol), XANTPHOS (0.549 g, 0.95 mmol) and SODIUM TERT-BUTOXIDE (2.129 g, 22.15 mmol) in toluene (125 mL) under nitrogen. The resulting mixture was stirred at 100 °C for 4 hours. The reaction mixture was evaporated to dryness and redissolved in EtOAc (100 mL), and washed sequentially with water (2 x 100 mL) and saturated brine (100 mL). The organic layer was dried over MgSO4, filtered and preadsorbed onto silica. The crude product was purified by flash silica chromatography, elution gradient 0 to 100% EtOAc in heptane. Pure fractions were evaporated to dryness to afford N-phenylpyridin-4-amine (1.102 g, 40.9 %) as a white solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-b128920e4d7f4cc2b5aeb697ff28a01f
출처 메모750 AstraZeneca ELN dataset