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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385592Generated: October 30, 2026

Sodium Bicarbonate → (5-Fluoro-6-(pyrrolidin-1-yl)pyridin-3-yl)methanol

https://huagongshe.com/reaction/385592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 5-fluoro-6-(pyrrolidin-1-yl)nicotinateHCID 57815379—
SolventTetrahydrofuranHCID 8028—
Product(5-Fluoro-6-(pyrrolidin-1-yl)pyridin-3-yl)methanolHCID 57815436111%

Reaction Steps

To a solution of 0.24 g of lithium aluminum hydride in 5 mL of THF, a solution of 0.70 g of methyl 5-fluoro-6-(pyrrolidin-1-yl)nicotinate in 5 mL of tetrahydrofuran was dropped under cooling with ice. After warming to room temperature, the mixture was stirred for 45 minutes, thereto was dropped a saturated aqueous sodium hydrogen carbonate solution under cooling with ice, and the mixture was stirred for 10 minutes. The reaction mixture was filtered, and the filtration residue was washed with ethyl acetate and water. The organic layer of the filtrate was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with water and a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 0.68 g of (5-fluoro-6-(pyrrolidin-1-yl)pyridin-3-yl)methanol as a brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-5163a8b65e4a4943b6d2e5e45336103a
Source noteuspto-grants-2013_02