تفاعل #52940
ord-31e592cc2df741b490f935ebab442950
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةthe mixture was refluxed for 1 day
- 2درجة الحرارةthe mixture was refluxed for another day
- 3تركيزThe mixture was then concentrated
- 4استخلاصextracted with CH2Cl2
- 5غسيلThe extract Was washed with sat. NaHCO3, water
- 6تجفيفdried (MgSO4)
- 7ترشيحfiltered
- 8أخرىevaporated
- 9أخرىThe residue was purified by preparative TLC (silica gel; eluent: hexane/AcOEt 5:1 to 2:1)
الإجراء التجريبي
N-(2,6-Dichlorobenzoyl)-4-(2,6-dimethoxyphenyl)-L-phenylalanine methyl ester (232 mg) was dissolved in anhydrous MeCN (10 mL) under N2 and 3,5-dichloro-1-fluoropyridinium triflate (85%, 353 mg) was added and the mixture was refluxed for 1 day. More 3,5-dichloro-1-fluoropyridinium triflate (175 mg) was added and the mixture was refluxed for another day. The mixture was then concentrated, and the residue was taken up with water and extracted with CH2Cl2. The extract Was washed with sat. NaHCO3, water, dried (MgSO4), filtered and evaporated. The residue was purified by preparative TLC (silica gel; eluent: hexane/AcOEt 5:1 to 2:1) to give N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxy-3-fluorophenyl)-L-phenylalanine methyl ester (109 mg) and N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxy-3,5-difluorophenyl)-L-phenylalanine methyl ester (37 mg).