Реакция #710491

ord-f5a02f319c614510b25985e63fc3ec89

Уравнение реакции

O
water
[BH4-].[Na+]
sodium borohydride
CCOC(=O)C(F)(F)c1ncc(Cl)cc1Cl
ethyl (3,5-dichloropyridin-2-yl)(difluoro)acetate
Cl
HCl
OCC(F)(F)c1ncc(Cl)cc1Cl
2-(3,5-dichloropyridin-2-yl)-2,2-difluoroethanol

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ЭкстракцияThe aequeous phase was extracted three times by 300 mL of ethyl acetate
  2. 2
    Промывкаthe organic phase was successively washed with brine, water
  3. 3
    Сушкаdried over magnesium sulfate
  4. 4
    ДругоеAfter evaporation of the solvent under vacuum 8.5 g of yellow oil
  5. 5
    Другоеwere obtained
  6. 6
    ФильтрацияAfter trituration in diisopropyl ether and filtration 6.8 g (80%) of 2-(3,5-dichloropyridin-2-yl)-2,2-difluoroethanol (Int-9)
  7. 7
    Другоеwere obtained as a white solid
  8. 8
    ДругоеMp (melting point)=56° C. (M+1)=228

Методика

To a solution of 10 g (37 mmol) of ethyl (3,5-dichloropyridin-2-yl)(difluoro)acetate (Int-7) in 60 mL of ethanol, were added portionwise at 0° C., 1.05 g (27.7 mmol) of sodium borohydride. The reaction mixture was stirred below 10° C. for 2 hours. 30 mL of 1 N HCl were then slowly added followed by 500 mL of water. The aequeous phase was extracted three times by 300 mL of ethyl acetate and the organic phase was successively washed with brine, water and dried over magnesium sulfate. After evaporation of the solvent under vacuum 8.5 g of yellow oil were obtained. After trituration in diisopropyl ether and filtration 6.8 g (80%) of 2-(3,5-dichloropyridin-2-yl)-2,2-difluoroethanol (Int-9) were obtained as a white solid. Mp (melting point)=56° C. (M+1)=228. 19F-NMR (235 MHz, CDCl3) δ (ppm): −105.85 (CF2).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09301526B2uspto-grants-2016_04