تفاعل #91113

ord-0bfeea6e0cdb4990ba64bd84abec8bee

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter the termination of the reaction
  2. 2
    درجة الحرارةthe reactant was cooled
  3. 3
    تركيزconcentrated under reduced pressure
  4. 4
    أخرىThe residue was purified by column chromatography (eluent, EtOAc/Hex=1/10)

الإجراء التجريبي

4-Benzyloxy-3,5-difluoro-benzaldehyde (1.2 g, 4.83 mmol) obtained in Step B and carbethoxymethylene triphenylphosphorane (2.0 g, 5.78 mmol) was dissolved in THF (10 mL), and the solution was stirred at 65˜75° C. for 1 hour. After the termination of the reaction, the reactant was cooled and concentrated under reduced pressure. The residue was purified by column chromatography (eluent, EtOAc/Hex=1/10) to obtain the title compound (1.2 g, 78%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09447044B2uspto-grants-2016_09