تفاعل #1973905

ord-9f05251ccfd64ff88a89785820fc93ad

معادلة التفاعل

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

المذيبات

ظروف التفاعل

درجة الحرارة
35°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08501038B2uspto-grants-2013_08