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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39608생성일: 2026년 10월 23일

3-Bromobiphenyl → Dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-YL)phosphine oxide

https://huagongshe.com/ko/reaction/39608

반응식

참여 물질

역할이름HCID투입량
반응물3-BromobiphenylHCID 16449—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물1,4-DioxaneHCID 31275—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
촉매palladium(II) acetateHCID 167845—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물Dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-YL)phosphine oxideHCID 67122844—

반응 조건

온도94 °C

반응 단계

To the mixture of 3-bromobiphenyl (0.020 ml, 0.12 mmol) and 1,4-dioxane (1.5 ml), water (0.15 ml), potassium phosphate tribasic n-hydrate (170 mg, 0.72 mmol), sodium 1,3-dioxo-1,3-dihydro-isoindole-2-ylmethyl trifluoroborate (60 mg, 0.24 mmol), palladium(II) acetate (2.7 mg, 0.012 mmol), and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (9.9 mg, 0.024 mmol) were added, and then the obtained reaction mixture was stirred at 94° C. (an outer temperature) overnight. The reaction mixture was cooled to room temperature, and then hydrazine hydrate (48 mg, 0.96 mmol) and methanol (2 ml) were added thereto, followed by heating to reflux for 40 min. The reaction mixture was cooled to room temperature, and then ethyl acetate and water were added to the reaction mixture, followed by filtration with celite. The organic layer of the filtrate was separated and washed with saline. The solvents were evaporated under reduced pressure from the organic layer, and then the obtained residue was purified with NH-silica gel column chromatography (ethyl acetate), thereby obtaining the entitled compound (11 mg, 51%) as the mixture with 2′-(dicyclohexyl-phosphinoyl)-2,6-dimethoxy-biphenyl (6.2 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524946B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8bc20bd6395941389bf10f1441644e6e
출처 메모uspto-grants-2013_09