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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1398180생성일: 2026년 10월 25일

Triethylamine → 6-[3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl]hex-5-yn-1-ol

https://huagongshe.com/reaction/1398180

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물5-Hexyn-1-olHCID 70234—
반응물1-(4-bromo-2-methoxyphenyl)-3-methyl-1H-1,2,4-triazoleHCID 66608977—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매Ethyl AcetateHCID 8857—
생성물6-[3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl]hex-5-yn-1-olHCID 66608834—

반응 조건

온도70 °C

반응 단계

A mixture of 1-(4-bromo-2-methoxyphenyl)-3-methyl-1H-1,2,4-triazole (3.00 g), 5-hexyn-1-ol (2.45 mL), dichlorobis(triphenylphosphine)palladium(II) (786 mg), copper(I) iodide (213 mg) and triethylamine (110 mL) was stirred at 70° C. for 14 hr, allowed to cool to room temperature, and diluted with ethyl acetate, and the mixture was filtered through celite. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.80 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901309B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-f3ecba20eb1a42cd96adf38eca5268e5
출처 메모uspto-grants-2014_12