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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493230Generated: October 30, 2026

Hydrochloric Acid → (2-Chloropyridin-4-yl)methanol

https://huagongshe.com/reaction/493230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-chloropyridine-4-carboxylateHCID 2736842—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTetrahydrofuranHCID 8028—
Product(2-Chloropyridin-4-yl)methanolHCID 706223795%

Reaction Steps

A 0.95 M solution of diisobutylaluminum hydride in hexane (200 mL, 190 mmol) was added dropwise to a solution of 2-chloroisonicotinic acid methyl ester (11 g, 62 mmol) in anhydrous tetrahydrofuran (300 mL) under a nitrogen atmosphere under ice-cooling, and then the mixture was stirred under ice-cooling for 2 hours. After that, 1 N hydrochloric acid (200 mL) was added thereto, the mixture was stirred at room temperature for 1 hour. A saturated aqueous sodium hydrogencarbonate solution (400 mL) was added to the reaction mixture, then the whole was extracted with ethyl acetate (100 mL) three times. The ethyl acetate layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure to give 8.5 g of the title reference compound as a white solid. (Yield 95%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534802B2
Source datasetuspto-grants-2009_05
ORD IDord-b2533e05012b4f1c9c094aaa74106879
Source noteuspto-grants-2009_05