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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl (3,5-dichloropyridin-2-yl)(difluoro)acetate | HCID 86732541 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3,5-Dichloropyridin-2-yl)-2,2-difluoroethan-1-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09301526B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-f5a02f319c614510b25985e63fc3ec89 |
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| Source note | uspto-grants-2016_04 |
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