تفاعل #88662
ord-1f8700ff20c5490587bd53da5f61a458
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةto cool to room temperature
- 2ترشيحThe resulting solid was collected by filtration
- 3أخرىThe obtained solid was purified by silica gel column chromatography (hexane
- 4workup.ADDITIONTo the obtained fraction was added a saturated aqueous sodium hydrogen carbonate solution
- 5استخلاصthe mixture was extracted with ethyl acetate
- 6تجفيفThe extract was dried over anhydrous magnesium sulfate
- 7تركيزconcentrated in vacuo
- 8أخرىrecrystallized from ethyl acetate
الإجراء التجريبي
A mixture of 3-(5-bromo-2-furyl)acryloyl azide (20.7 g), diphenyl ether (200 mL) and tributylamine (16 mL) was stirred at 220-230° C. for 30 min under a nitrogen atmosphere. The reaction mixture was allowed to cool to room temperature, and tert-butyl methyl ether (200 mL) was added thereto. The resulting solid was collected by filtration. The obtained solid was purified by silica gel column chromatography (hexane, then ethyl acetate/THF), followed by HPLC (C18, mobile phase: water/acetonitrile (including 0.1% TFA)). To the obtained fraction was added a saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, concentrated in vacuo, and recrystallized from ethyl acetate to give the title compound (7.00 g) as a white solid.