تفاعل #1973900

ord-822928ce188b4f22a71b859fea989224

معادلة التفاعل

CCCCOc1ccc(C2CCC3(CC2)OCCO3)c(F)c1F
compound ( 10 )
CCCCOc1ccc(C2CCC3(CC2)OCCO3)c(F)c1F
8-(4-butoxy-2,3-difluorophenyl)-1,4-dioxaspiro[4.5]decane
O=CO
formic acid
O
water
CCCCOc1ccc(C2CCC(=O)CC2)c(F)c1F
1-(4-butoxy-2,3-difluorophenyl)-cyclohexan-4-one
المردود 97.7%

المذيبات

ظروف التفاعل

درجة الحرارة
30°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was heated
  2. 2
    درجة الحرارةto reflux for 2 hours
  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
    تجفيفa saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate
  9. 9
    workup.DISTILLATIONThe solvent was then distilled off under reduced pressure
  10. 10
    أخرىthe resulting residue was purified with a fractional operation by means of column chromatography
  11. 11
    أخرىThe product was further purified by recrystallization from heptane

الإجراء التجريبي

The compound (10) (47.8 g), formic acid (87%; 67.0 ml) and toluene (200 ml) were mixed, and the mixture was heated to reflux for 2 hours. After the reaction mixture had been cooled to 30° C., water (500 ml) and toluene (1,000 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, a saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure and the resulting residue was purified with a fractional operation by means of column chromatography using silica gel as a stationary phase powder and toluene as an eluent. The product was further purified by recrystallization from heptane to give 1-(4-butoxy-2,3-difluorophenyl)-cyclohexan-4-one (11) (40.4 g). The yield based on the compound (10) was 97.8%.

المصدر

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