돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39607생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/39607

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-BromoanisoleHCID 11358—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
촉매palladium(II) acetateHCID 167845—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물Dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-YL)phosphine oxideHCID 6712284445.4%

반응 조건

온도95 °C

반응 단계

To the mixture of 2-bromoanisole (0.020 ml, 0.16 mmol) and 1,4-dioxane (2 ml), water (0.2 ml), cesium carbonate (0.32 g, 0.97 mmol), sodium 1,3-dioxo-1,3-dihydro-isoindole-2-ylmethyl trifluoroborate (81 mg, 0.32 mmol), palladium(II) acetate (3.6 mg, 0.016 mmol), and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (13 mg, 0.032 mmol) were added, and then the obtained reaction mixture was stirred at 95° C. (an outer temperature) overnight. The reaction mixture was cooled to room temperature, and then hydrazine hydrate (0.039 ml, 0.81 mmol) and methanol (2 ml) were added thereto, followed by heating to reflux for 1 hour. The reaction mixture was cooled to room temperature, and then water and ethyl acetate 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 (heptane:ethyl acetate=1:4), thereby obtaining the entitled compound (4.1 mg, 19%) 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-d01713c474f74d42b87c525175407e98
출처 메모uspto-grants-2013_09