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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632952Generated: October 27, 2026

Acetone → (3-(Benzyloxy)pyridin-2-yl)methanol

https://huagongshe.com/reaction/1632952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
Reactant3-Hydroxy-2-(hydroxymethyl)pyridine hydrochlorideHCID 3084185—
SolventWaterHCID 962—
Product(3-(Benzyloxy)pyridin-2-yl)methanolHCID 13217540104.9%

Reaction Steps

Sodium hydroxide (31.5 grams, 0.78 mole) was dissolved in 100 ml water and 100 ml of acetone was added followed by 3-hydroxy-2(hydroxymethyl)pyridine hydrochloride (63.8 grams; 0.39 mole). 250 ml of acetone was added followed by benzyl bromide (74.1 grams; 51.5 ml; 0.43 mole). The mixture was refluxed for a period of 4.5 hours and the acetone evaporated in vacuo. The aqueous layer was extracted with CH2Cl2 (three times 150 ml) and the extracts dried (anhydrous Na2SO4) and concentrated to yield 88.1 grams of a brown liquid. The brown liquid (88.1 grams) was dissolved in ether and ether-HCl added to form the hydrochloride salt. The HCl salt was filtered and the filter cake dissolved in water. The aqueous solution was basified to afford a brown pasty precipate which on trituration with ether afforded 58.7 grams of material. Recrystallization from ethanol yielded 31.6 grams of a tan solid, m.p. 79°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04478834
Source datasetuspto-grants-1984_10
ORD IDord-320bf9524af545fd81f3ebb3ca2584f0
Source noteuspto-grants-1984_10