تفاعل #1144433

ord-037a4671fd454eaea8e1b443c297112d

المذيبات

ظروف التفاعل

درجة الحرارة
-70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise over 15 minutes
  2. 2
    أخرىto react for 20 minutes
  3. 3
    أخرىbrought to room temperature
  4. 4
    غسيلThe mixture was washed with water (3 ml×5) and saturated aqueous solution of sodium hydrogencarbonate (twice),
  5. 5
    أخرىdried on magnesium sulfate
  6. 6
    تركيزconcentrated under reduced pressure
  7. 7
    أخرىThe residue was purified by silica gel chromatography (ethyl acetate/hexane=3:17)
  8. 8
    أخرىcrystallized from ethyl acetate

الإجراء التجريبي

Then, 3.3 ml lithium diisopropylamide solution in tetrahydrofuran (2.1M) was added to 9 ml of tetrahydrofuran under a nitrogen atmosphere at −70° C., to which a solution of 0.56 g (3.0 mmol) of 1-ethoxymethyl-2-thiouracil in 3 ml of tetrahydrofuran was added dropwise over 15 minutes. After stirring for 1 hour at −70° C., the reaction mixture was added with a solution of 0.85 g (3.9 mmol) of diphenyl disulfide in 1 ml of tetrahydrofuran dropwise over 10 minutes and allowed to react for 20 minutes. The reaction mixture was added with 1 ml of acetic acid, brought to room temperature and then added with 30 ml of ethyl acetate. The mixture was washed with water (3 ml×5) and saturated aqueous solution of sodium hydrogencarbonate (twice), dried on magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/hexane=3:17), crystallized from ethyl acetate to obtain 0.64 g of 1-ethoxymethyl-6-phenylthio-2-thiouracil (Yield: 73%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE037979E1uspto-grants-2003_02