돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71210생성일: 2026년 10월 23일

Triethylamine → 5-[4-(5-Chloropent-1-yn-1-yl)-2-methoxyphenyl]-2-methyl-1,3-oxazole

https://huagongshe.com/ko/reaction/71210

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Pentyne, 5-chloro-HCID 84308—
반응물5-(4-Bromo-2-methoxyphenyl)-2-methyloxazoleHCID 66608732—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매Ethyl AcetateHCID 8857—
생성물5-[4-(5-Chloropent-1-yn-1-yl)-2-methoxyphenyl]-2-methyl-1,3-oxazoleHCID 66608267—

반응 조건

온도70 °C

반응 단계

A mixture of 5-(4-bromo-2-methoxyphenyl)-2-methyl-1,3-oxazole (6.00 g), 5-chloropent-1-yne (4.74 mL), dichlorobis(triphenylphosphine)palladium(II) (1.57 g), copper(I) iodide (426 mg) and triethylamine (60 mL) was stirred at 70° C. for 3 hr, 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 (4.85 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822699B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4cc6270886fc4692977c650aa62d336b
출처 메모uspto-grants-2014_09