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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172637Generated: November 1, 2026

Ammonium Chloride → (3,5-Difluoropyridin-2-YL)methanol

https://huagongshe.com/reaction/2172637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 3,5-difluoropyridine-2-carboxylateHCID 46311358—
SolventEthanolHCID 702—
Product(3,5-Difluoropyridin-2-YL)methanolHCID 5341431498.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3,5-difluoro-pyridine-2-carboxylic acid ethyl ester of Step A (2.5 g, 12.6 mmol) in ethanol (10 mL), cooled using an ice water bath, was added sodium borohydride (1.43 g, 37.8 mmol) in a portion wise manner. The solution was stirred at 0° C. for thirty minutes and at ambient temperature for two hours. The reaction was returned to 0° C. and saturated ammonium chloride was added dropwise. The solvent was removed in vacuo and the resulting residue was partitioned between ethyl acetate and water. The organic layer was washed with saturated ammonium chloride, water and brine and dried over magnesium sulfate. The slurry was filtered and concentrated to provide the alcohol as a yellow oil (1.8 g, 98%). MS (M+H): 146

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056110B2
Source datasetuspto-grants-2015_06
ORD IDord-784d3e8868404d2fbf34d29aced4186d
Source noteuspto-grants-2015_06