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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240168생성일: 2026년 10월 25일

3-Bromoaniline → 3-(1H-Pyrazol-3-yl)aniline

https://huagongshe.com/reaction/240168

반응식

참여 물질

역할이름HCID투입량
반응물3-BromoanilineHCID 11562—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물TricyclohexylphosphineHCID 75806—
반응물1H-Pyrazole-5-boronic acidHCID 11251979—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물3-(1H-Pyrazol-3-yl)anilineHCID 273539820%

반응 단계

1H-pyrazole-5-boronic acid (0.072 g, 0.639 mmol) and 3-bromoaniline (0.063 mL, 0.581 mmol) were combined in dioxane (2 mL) in a flame-dried, round-bottom flask. K3PO4 (1.27M, 0.778 mL, 0.99 mmol), PCy3 (0.004 g, 0.014 mmol), and Pd2(dba)3 (0.005 g, 0.006 mmol) were added to the stirred solution. The reaction was refluxed overnight under argon flow, and subsequently cooled to room temperature. The solvent was removed under vacuum and the resulting residue was resuspended in CH2Cl2. The organic phase was dried over MgSO4, filtered, and concentrated under vacuum. The crude product was purified by flash silica column chromatography (70-100% EtOAc/hexanes). The purification was monitored by TLC. The solvent was removed under vacuum from fractions containing product, resulting in 0.018 g in 20% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642788B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-95666a464a764a6eb78e00dfa43597f5
출처 메모uspto-grants-2014_02