تفاعل #412212
ord-f3efa4e37f874cebb02fd3f8e54d0e7d
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1ترشيحAfter filtration through Celite the solvent
- 2أخرىwas evaporated
- 3أخرىThe residue was purified by preparative HPLC (60% CH3CN/aq:0.1M NH4OAc)
الإجراء التجريبي
A suspension of 3-[2-(4-amino{t-butoxycarbonylimino}methylphenyl)-ethoxy]nitrobenzene (1.47 g; 3.81 mmol; from step (iii) above) and Pd (0.236 g; 5% on charcoal) in EtOH (75 mL) was stirred under H2(g) (1 atm.) for 25 minutes. After filtration through Celite the solvent was evaporated. The residue was purified by preparative HPLC (60% CH3CN/aq:0.1M NH4OAc) to afford the sub-title compound. Yield: 1.02 g (75%).