تفاعل #2139944
ord-6335e2f2f40b4d0ba02708c43848d337
معادلة التفاعل
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGthe mixture was stirred for a further 5 minutes
- 2ترشيحThe reaction mixture was filtered through Celite® with suction
- 3أخرىthe phases were separated
- 4استخلاصThe aqueous phase was extracted twice with MTB ether
- 5غسيلthe combined organic phases were washed three times with water
- 6تجفيفdried over sodium sulfate
- 7أخرىevaporated under reduced pressure
- 8ترشيحThe crude product was filtered through silica gel with n-heptane
الإجراء التجريبي
190 g (0.600 mol) of 4-bromo-2-fluoro-1-iodobenzene and 65.3 ml of 1-pentyne were dissolved in a mixture of 900 ml of THF and 1.2 l of triethylamine and cooled to 10° C., and 1.14 g (6 mmol) of copper(I) iodide and 8.42 g (12 mmol) of bis(triphenylphosphine)palladium(II) chloride were added. The batch was stirred overnight at room temperature, water and MTB ether were subsequently added, and the mixture was stirred for a further 5 minutes. The reaction mixture was filtered through Celite® with suction, and the phases were separated. The aqueous phase was extracted twice with MTB ether, and the combined organic phases were washed three times with water, dried over sodium sulfate and evaporated under reduced pressure. The crude product was filtered through silica gel with n-heptane, giving 129 g of 4-bromo-2-fluoro-1-pent-1-ynylbenzene as a yellow liquid. Hydrogenation on palladium/activated carbon (10%) in THF gave 131 g (100%) of 4-bromo-2-fluoro-1-pentylbenzene as a yellow liquid.