تفاعل #49721

ord-e8829847a21247b7b70fa8f2b5cf2745

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe reaction mixture was heated at 100°-110° C.
  2. 2
    workup.STIRRINGwith stirring for 3 hours
  3. 3
    درجة الحرارةAfter cooling
  4. 4
    استخلاصextracted with ethyl acetate
  5. 5
    أخرىThe organic layer separated from the aqueous layer
  6. 6
    غسيلwas washed with aqua
  7. 7
    تجفيفsaturated sodium chloride solution three times and the organic layer was dried over anhydrous magnesium sulfate
  8. 8
    أخرىThe solvent was removed under reduced pressure
  9. 9
    أخرىthe residue obtained

الإجراء التجريبي

2.41 Grams of 60% sodium hydride in oil was suspended in 100 ml of N,N-dimethylformamide and to the suspension was added gradually 17.44 g of benzyl 6-phenylsalicylate dissolved in 50 ml of N,N-dimethylformamide. Then, the mixture was stirred at room temperature for 30 minutes. To the reaction system was added 10.01 g of 4-chloro-2,6-dimethoxypyrimidine in 50 ml of N,N-dimethylformamide and the reaction mixture was heated at 100°-110° C. with stirring for 3 hours. After cooling on standing, the reaction mixture was poured into 1N hydrochloric acid and extracted with ethyl acetate. The organic layer separated from the aqueous layer was washed with aqua. saturated sodium chloride solution three times and the organic layer was dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue obtained was subjected to silica gel column chromatography (hexane/ethyl acetate (10:1-3:1, v/v) to obtain 21.55 g of benzyl 2-(2,6-dimethoxypyrimidine-4-yloxy)-6-phenylbenzoate.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05424275uspto-grants-1995_06