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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271503생성일: 2026년 10월 24일

Triphenylphosphine → 2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/ko/reaction/271503

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물TrimethylsilylacetyleneHCID 66111—
반응물2-Chloro-4-iodopyridineHCID 1516511—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridineHCID 21985391—

반응 단계

2-Chloro-4-iodo-pyridine (10.0 g, 41.8 mmol) was dissolved in 200 mL dry THF and 17.5 mL triethyl amine. This mixture was evacuated and backfilled with argon several times to remove oxygen from the solution. Triphenylphosphine (329 mg, 1.25 mmol) and bis(triphenylphosphine)palladium(II)chloride (1.47 g, 2.09 mmol) were added and the reaction mixture was stirred at room temperature for 1 h. Copper(I)iodide (239 mg, 1.25 mmol) and trimethylsilylacetylene (6.28 g, 6.39 mmol) were added. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated. The residue was taken up in 500 mL water and extracted three times with ethyl acetate (500 mL each). The combined organic extracts were dried with magnesium sulfate, filtered and evaporated. The crude product was purified by chromatography on silica gel (cyclohexane/ethyl acetate 80:20). The desired product was obtained as a light brown semi solid (10 g, >100%). This material was used without any further purification for the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452909B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-1e2bfc7e92b4444bb4badf530398ff26
출처 메모uspto-grants-2008_11