تفاعل #67886
ord-8bc20bd6395941389bf10f1441644e6e
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwere added
- 2أخرىthe obtained reaction mixture
- 3درجة الحرارةThe reaction mixture was cooled to room temperature
- 4درجة الحرارةby heating
- 5درجة الحرارةto reflux for 40 min
- 6درجة الحرارةThe reaction mixture was cooled to room temperature
- 7ترشيحfollowed by filtration with celite
- 8أخرىThe organic layer of the filtrate was separated
- 9غسيلwashed with saline
- 10أخرىThe solvents were evaporated under reduced pressure from the organic layer
- 11أخرىthe obtained residue was purified with NH-silica gel column chromatography (ethyl acetate)
الإجراء التجريبي
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).