تفاعل #1132855

ord-26eebf93143842268c8112a5ff7decad

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter removal of the solvent, hydrochloric acid
  2. 2
    workup.ADDITIONwas added
  3. 3
    أخرىthe resulting solution was partitioned between water and ethyl acetate
  4. 4
    غسيلThe organic layer was washed with brine
  5. 5
    تجفيفdried over sodium sulfate
  6. 6
    أخرىThe solvent was removed under reduced pressure
  7. 7
    أخرىthe residue was purified with silica gel column chromatography (eluent; hexane/ethyl acetate=2/1)

الإجراء التجريبي

A solution of 2-phenyl-pyrimidine-4-carboxylic acid (3.49 g, 17.4 mmol) and 1,1′-carbonyldiimidazole (2.86 g, 17.7 mmol) in tetrahydrofuran (100 ml) was stirred at 60° C. for 20 min. After cooling to room temperature, ethyl potassium malonate (3.28 g, 19.2 mmol) and magnesium chloride (2.48 g, 26.1 mmol) were added and the solution was stirred at 60° C. for 7 hours. After removal of the solvent, hydrochloric acid was added to adjust pH to 4 to 2, and the resulting solution was partitioned between water and ethyl acetate. The organic layer was washed with brine and dried over sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified with silica gel column chromatography (eluent; hexane/ethyl acetate=2/1) to afford 3-oxo-3-(2-phenyl-pyrimidin-4-yl)-propionic acid ethyl ester (2.74 g, 58%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08569294B2uspto-grants-2013_10