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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606845생성일: 2026년 10월 25일

Cesium carbonate → 3-Trifluoromethyl-5-phenylethynylpyridine

https://huagongshe.com/reaction/606845

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물PhenylacetyleneHCID 10821—
반응물3-Chloro-5-(trifluoromethyl)pyridineHCID 2736698—
촉매Bis(acetonitrile)dichloropalladiumHCID 6093782—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물3-Trifluoromethyl-5-phenylethynylpyridineHCID 6704770310%

반응 단계

Charge a sealed tube under a positive pressure of argon with bis(acetonitrile)palladium (II) chloride (18 mg, 0.07 mmol), 2-dicyclohexylphosphino diphenyl (73 mg, 0.21 mmol), cesium carbonate (0.557 g, 1.71 mmol) and 3-chloro-5-trifluoromethylpyridine, (prepared essentially as described in PREPARATION 7), (0.12 g, 0.66 mmol) in acetonitrile and stir at room temperature for 25 min (Angew. Chem. Int. Ed. 42, 5993-5996, (2003)). Add phenylacetylene (0.1 mL, 0.86 mmol) and stir at 100° C. for 16 h. Cool to room temperature, dilute with water, and wash twice with ethyl acetate. Combine the ethyl acetate layers, dry (sodium sulfate), and concentrate. Purify the residue by silica gel chromatography, eluting with 100:0 to 50:50 hexanes:dichloromethane, to obtain the title compound (30 mg, 10%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915424B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c56a8d459fa94d37b179bea42a95c2e4
출처 메모uspto-grants-2011_03