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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1271301생성일: 2026년 10월 27일

2-(4-Pentynyloxy)tetrahydro-2H-pyran → 5,6-Diphenyl-2-[5-(2-tetrahydropyranyloxy)-1-pentyn-1-yl]pyrazine

https://huagongshe.com/reaction/1271301

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Pentynyloxy)tetrahydro-2H-pyranHCID 357816—
반응물5-Chloro-2,3-DiphenylpyrazineHCID 3654493—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TriethylamineHCID 8471—
생성물5,6-Diphenyl-2-[5-(2-tetrahydropyranyloxy)-1-pentyn-1-yl]pyrazineHCID 2293195575.8%

반응 조건

온도80 °C

반응 단계

To a solution of 1.58 g of 2-chloro-5,6-diphenylpyrazine in 10 ml of triethylamine, 1.20 g of 5-(2-tetrahydropyranyloxy)-1-pentyne, 208 mg of dichlorobis(triphenylphosphine)palladium (II) and 56 mg of copper (I) iodide were added, followed by stirring under an argon atmosphere at 80° C. for 8 hours. The solvent was evaporated under reduced pressure and the residue was dissolved in diethyl ether, and then the insoluble matter was removed by filtration through celite. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography to obtain 1.79 g of the desired compound as a brown oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07205302B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-30c9cb5a484e4641a505c92c2d64f0e7
출처 메모uspto-grants-2007_04