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HRID 39607生成日期:2026年10月23日

碳酸氢铯 → Dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-YL)phosphine oxide

https://huagongshe.com/zh-CN/reaction/39607

反应方程式

参与物

角色名称HCID投料
反应物碳酸氢铯HCID 10796—
反应物2-溴苯甲醚HCID 11358—
反应物水合肼HCID 24654—
反应物2-双环己基膦-2',6'-二甲氧基联苯HCID 11269872—
催化剂palladium acetateHCID 167845—
溶剂(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮HCID 887—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
溶剂乙酸乙酯HCID 8857—
溶剂1,4-二氧六环HCID 31275—
产物Dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-YL)phosphine oxideHCID 6712284445.4%

反应条件

温度95 °C

反应步骤

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).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08524946B2
来源数据集uspto-grants-2013_09
ORD IDord-d01713c474f74d42b87c525175407e98
来源说明uspto-grants-2013_09