반응 #1973905

ord-9f05251ccfd64ff88a89785820fc93ad

반응 방정식

Cc1ccccc1
toluene
CCOc1ccc([C@H]2CC[C@H](C=O)CC2)c(F)c1F
compound ( 16 )
CCOc1ccc([C@H]2CC[C@H](C=O)CC2)c(F)c1F
trans-4-(4-Ethoxy-2,3-difluorophenyl)-cyclohexanecarboaldehyde
CC(C)=O
acetone
CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones reagent
CCOC1(C(=O)O)CCC[C@@H](F)[C@@H]1F
4-ethoxy-2,3-difluoro-(trans-4-cyclohexyl)-carboxylic acid

용매

반응 조건

온도
35°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe mixture was stirred at 35° C. for 2 hours
  2. 2
    온도After the reaction mixture had been cooled to 30° C.
  3. 3
    workup.ADDITIONmixed with it
  4. 4
    기타had separated into two phases of organic and aqueous phases
  5. 5
    추출the extraction into an organic phase
  6. 6
    기타The resulting organic phase was separated
  7. 7
    세척washed successively with water
  8. 8
    건조an aqueous solution of sodium thiosulfate and water, and then dried over anhydrous magnesium sulfate

실험 절차

The compound (16) (10.0 g) and acetone (50 ml) were mixed and the mixture was stirred at 35° C. for 30 minutes. Jones reagent (8N) (4.7 ml) was added to the mixture in the temperature range of 30 to 40° C. and the mixture was stirred at 35° C. for 2 hours. After the reaction mixture had been cooled to 30° C., toluene (200 ml) and water (200 ml) were added to the mixture and mixed with it. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases, and the extraction into an organic phase was carried out. The resulting organic phase was separated, and washed successively with water, an aqueous solution of sodium thiosulfate and water, and then dried over anhydrous magnesium sulfate, giving 4-ethoxy-2,3-difluoro-(trans-4-cyclohexyl)-carboxylic acid (31) (8.8 g). The yield based on the compound (16) was 83.1%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08501038B2uspto-grants-2013_08