돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2273972생성일: 2026년 10월 27일

Borane → 3-Bromo-5-chlorophenol

https://huagongshe.com/reaction/2273972

반응식

참여 물질

역할이름HCID투입량
반응물BoraneHCID 6331—
반응물1-Bromo-3-chlorobenzeneHCID 7928—
반응물1,2-Bis(dimethylphosphino)ethaneHCID 141059—
반응물PinacolboraneHCID 6364989—
반응물Potassium hydroxy sulfiteHCID 23707502—
촉매(1,5-cyclooctadiene)-eta5-indenyl)iridium(I)HCID 178420247—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물3-Bromo-5-chlorophenolHCID 2263018062%

반응 조건

온도150 °C

반응 단계

Under an atmosphere of dry nitrogen, 103 mg 1,5-cyclooctadiene(H5-indenyl)iridium (I) was put in a 25 mL Pyrex bottle. Subsequently were added 0.04 mL 1,2-bis(dimethylphosphino)ethane, 0.61 mL 3-bromochlorobenzene and 1.52 mL pinacolborane. The mixture was stirred at 150° C. for 3.5 h. After cooling to room temperature, the borane adduct was taken up in 17 mL acetone to give a clear solution. This solution was added slowly to 17.41 mL of a 0.30 M solution of oxone in water cooled in an ice bath. The mixture was stirred vigorously for 15 min. at room temperature and extracted three times with DCM. The combined organic phases were dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (DCM) to yield 750 mg (62%) of a beige solid. 1H NMR complies with known data (compound (1), Maleczka, 2003).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09126942B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-a5a2626f91834e989eac6b6c555d3aa3
출처 메모uspto-grants-2015_09