Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385563Generated: October 30, 2026

Sodium Bicarbonate → (5-Fluoro-6-methoxypyridin-3-yl)methanol

https://huagongshe.com/reaction/385563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 5-fluoro-6-methoxynicotinateHCID 46311253—
SolventTetrahydrofuranHCID 8028—
Product(5-Fluoro-6-methoxypyridin-3-yl)methanolHCID 57815441111.7%

Reaction Steps

To a suspension of 0.24 g of lithium aluminum hydride in 6 mL of tetrahydrofuran, a solution of 0.58 g of methyl 5-fluoro-6-methoxynicotinate in 3.5 mL of tetrahydrofuran was dropped under cooling with ice. After warming to room temperature, the mixture was stirred for 30 minutes. Thereto was dropped a saturated aqueous sodium hydrogen carbonate solution under cooling with ice, after stirring for 10 minutes, the reaction mixture was filtered through celite, 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 0.55 g of (5-fluoro-6-methoxypyridin-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-0706982113ad42619dd254da72fa5a56
Source noteuspto-grants-2013_02