تفاعل #86797

ord-1b48d87923584885ad5320c3ae2d22c0

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed with n-hexane
  2. 2
    أخرىto prepare an aqueous solution of sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate
  3. 3
    أخرىan organic layer was isolated
  4. 4
    غسيلwashed with water
  5. 5
    تركيزwas concentrated under reduced pressure
  6. 6
    workup.ADDITIONMethylisobutyl ketone was added to the concentrated solution
  7. 7
    تركيزconcentrated again
  8. 8
    workup.ADDITIONDiisopropyl ether was added to the concentrated solution for crystallization
  9. 9
    أخرىa solid obtained
  10. 10
    أخرىwas dried under reduced pressure

الإجراء التجريبي

After stirring a mixed solution of 1-adamantane carboxylic acid 2-ethoxycarbonyl-2,2-difluoro-1-phenyl-ethyl ester (6.6 g) prepared in Synthesis Example 1-5, 1-4-dioxane (20 g) and 25% by mass of caustic soda (2.5 g) for 2 hours, water (30 g) was added to the reaction solution and washed with n-hexane to prepare an aqueous solution of sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate. An aqueous solution of 4-tert-butyl phenyldiphenylsulfonium methyl sulfate (95 g) and methylene chloride (100 g) were added to the product, stirred for 30 minutes, and then an organic layer was isolated and washed with water, and thereafter was concentrated under reduced pressure. Methylisobutyl ketone was added to the concentrated solution, and concentrated again. Diisopropyl ether was added to the concentrated solution for crystallization, and a solid obtained was dried under reduced pressure to obtain a target compound, or 4-tert-butylphenyldiphenyl sulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate (5.4 g) as a white crystal (yield: 52%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09436083B2uspto-grants-2016_09