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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891830Generated: November 1, 2026

Dimethylformamide → 5-(Benzyloxy)-2-methylpyridine

https://huagongshe.com/reaction/1891830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
Product5-(Benzyloxy)-2-methylpyridineHCID 1239725166%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an N,N-dimethylformamide (50 mL) solution of 3-hydroxy-6-methylpyridine (5.00 g, 45.8 mmol) was added sodium hydride (2.02 g, 50.4 mmol, 60% in oil), which was stirred for 15 minutes at 0° C. Next, benzyl bromide (5.99 mL, 50.4 mmol) was added to this reaction mixture at 0° C., which was stirred for 3.5 hours at room temperature. Water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=2:1) to obtain the tile compound (5.99 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-e93b71380450411aa3c33ce14ad12ba7
Source noteuspto-grants-2013_08