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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623309Generated: October 29, 2026

Hydrochloric Acid → 2-(3,5-Dichloropyridin-2-yl)-2,2-difluoroethan-1-ol

https://huagongshe.com/reaction/623309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl (3,5-dichloropyridin-2-yl)(difluoro)acetateHCID 86732541—
SolventEthanolHCID 702—
Product2-(3,5-Dichloropyridin-2-yl)-2,2-difluoroethan-1-olHCID 86732542—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301526B2
Source datasetuspto-grants-2016_04
ORD IDord-f5a02f319c614510b25985e63fc3ec89
Source noteuspto-grants-2016_04