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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60658생성일: 2026년 10월 24일

1-Bromo-3-chlorobenzene → 3-Bromo-5-chlorophenol

https://huagongshe.com/ko/reaction/60658

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-3-chlorobenzeneHCID 7928—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물Potassium hydroxy sulfiteHCID 23707502—
촉매(1,5-Cyclooctadiene)(methoxy)iridium(I) dimerHCID 53216975—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물3-Bromo-5-chlorophenolHCID 22630180134.9%

반응 단계

A flask containing (1,5-cyclooctadiene)(methoxy)-iridium(I) dimer (84 mg, 0.13 mmol), 4,4′-di-tert butyl-2-2′-dipyridyl (69 mg, 0.26 mmol) and bis(pinacolato)diboron (1.29 g, 5.11 mmol) was purged with Ar, then hexanes (26 mL) and 1-bromo-3-chlorobenzene (1 mL, 8.51 mmol) were added sequentially. The solution was stirred at RT for 18 h. The reaction mixture was concentrated in vacuo, re-dissolved in acetone (26 mL), then oxone (5.23 g, 8.51 mmol) in water (26 mL) added [Caution: exotherm observed]. After 10 min, the reaction mixture was diluted with DCM. The layers separated, and the aqueous layer extracted with DCM. The combined organics were washed with brine, dried and concentrated in vacuo to give the title compound (1.43 g, 81%). LCMS (Method 3): Rt 3.74 min, m/z 205, 207 [M-H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440974B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-e7b420fca4cd44b99f56ad6c52a98cc7
출처 메모uspto-grants-2016_09