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HRID 39608作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromobiphenylHCID 16449—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物1,4-DioxaneHCID 31275—
反応物2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
触媒palladium(II) acetateHCID 167845—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物Dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-YL)phosphine oxideHCID 67122844—

反応条件

温度94 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524946B2
出典データセットuspto-grants-2013_09
ORD IDord-8bc20bd6395941389bf10f1441644e6e
出典メモuspto-grants-2013_09