돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 879916생성일: 2026년 10월 25일

1,2-Diaminocyclohexane, trans- → 3-bromo-9-(dibenzo[b,d]furan-2-yl)-9H-carbazole

https://huagongshe.com/reaction/879916

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Diaminocyclohexane, trans-HCID 43806—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-IododibenzofuranHCID 223327—
반응물3-BromocarbazoleHCID 252446—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매1,4-DioxaneHCID 31275—
생성물3-bromo-9-(dibenzo[b,d]furan-2-yl)-9H-carbazoleHCID 5851100156.3%

반응 단계

A mixture of 8.9 g (36.2 mmole) 3-bromo-9H-carbazole, 10.6 g (36.2 mmole) of 2-iododibenzo[b,d]furan, 17.1 g (90 mmole) of copper(I) iodide, 19.1 g (90 mmole) of potassium phosphate, 10.3 g (90 mmole) of trans-1,2-cyclohexanediamine and 1,4-dioxane 700 ml were refluxed under nitrogen for about overnight. Then, the solution was filtered at 110° C. To receive the filtrate, And the 1,4-dioxane was removed under reduced pressure from the filtrate. The filtrate was extracted with 500 ml dichloromethane and 2000 ml water, the organic layer was dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-ethyl acetate) to give product 8.4 g (56%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993130B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-8a9db235b26c47ad9e6e87a852b08f9e
출처 메모uspto-grants-2015_03