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HRID 1877456생성일: 2026년 10월 27일

Dichloromethane → [5-(9H-carbazol-4-yl)pyridin-2-yl]methanol

https://huagongshe.com/reaction/1877456

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Cesium carbonateHCID 10796—
반응물6-(Hydroxymethyl)pyridine-3-boronic acidHCID 44118255—
반응물4-TrifluoromethanesulphonyloxycarbazoleHCID 58338323—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물[5-(9H-carbazol-4-yl)pyridin-2-yl]methanolHCID 6730875547.4%

반응 단계

0.54 g of [6-(hydroxymethyl)pyridin-3-yl]boronic acid, 3.3 g of caesium carbonate and 93 mg of 1,1′-bis(diphenylphosphino)ferrocenepalladium(II) dichloride as a complex with dichloromethane (1/1) [PdCl2(dppO'CH2Cl2] are successively added, under argon, to a solution of 0.8 g of 4-trifluoromethanesulphonyloxycarbazole, obtained in stage 1 of Example 1, in a mixture of 37 ml of dioxane and 12 ml of water. The reaction mixture is refluxed for 5 hours, cooled to ambient temperature and concentrated under reduced pressure. The residue is subsequently taken up with a mixture of dichloromethane and ethyl acetate, treated with carbon black, filtered through celite and concentrated under reduced pressure. The residue is purified by silica gel chromatography, elution being carried out with a mixture of cyclohexane and ethyl acetate (55/45 by volume), so as to give 0.33 g of [5-(9H-carbazol-4-yl)pyridin-2-yl]methanol in the form of a colourless oil, the characteristics of which are the following:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309721B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-07590bc6edc9417d90f7d425d358aa4b
출처 메모uspto-grants-2012_11