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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1916721생성일: 2026년 10월 23일

Triethylamine → HCID 69076337, 화합물

https://huagongshe.com/ko/reaction/1916721

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(Di-tert-butylphosphino)biphenylHCID 2734215—
반응물3-(5-Bromopyridin-2-yl)prop-2-yn-1-olHCID 13979730—
반응물p-Chlorophenylboric acidHCID 17810664—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 69076337HCID 69076337—

반응 조건

온도60 °C

반응 단계

Under an N2 atmosphere 1 mL (7.22 mmol) triethylamine, 23 mg (0.1 mmol) Pd(OAc)2 and 57.5 mg (0.19 mmol) biphenyl-2-yl-di-tert-butyl-phosphane are added to a solution of 500 mg (2.36 mmol) 3-(5-bromo-pyridin-2-yl)-prop-2-yn-1-ol and 600 mg (3.72 mmol) 4-chlorophenyl-boric acid in 10 mL DMF and 2.5 mL water and the reaction mixture is stirred for 8 h at 60° C. Then 400 mg (2.48 mmol) 4-chlorophenyl-boric acid are added and the mixture is stirred for a further 19 h at 60° C. The mixture is evaporated down i. vac., the residue is combined with 10 mL water and 10 mL EtOAc, the aqueous phase is saturated with NaCl, the organic phase is separated off and dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified by chromatography (silica gel, cyc/EtOAc3 2:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08618132B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-e96886e555c64fa6a9d8e7dd566e04f0
출처 메모uspto-grants-2013_12