반응 #49721

ord-e8829847a21247b7b70fa8f2b5cf2745

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the reaction mixture was heated at 100°-110° C.
  2. 2
    workup.STIRRINGwith stirring for 3 hours
  3. 3
    온도After cooling
  4. 4
    추출extracted with ethyl acetate
  5. 5
    기타The organic layer separated from the aqueous layer
  6. 6
    세척was washed with aqua
  7. 7
    건조saturated sodium chloride solution three times and the organic layer was dried over anhydrous magnesium sulfate
  8. 8
    기타The solvent was removed under reduced pressure
  9. 9
    기타the residue obtained

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05424275uspto-grants-1995_06