반응 #710491

ord-f5a02f319c614510b25985e63fc3ec89

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09301526B2uspto-grants-2016_04