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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691221Generated: October 29, 2026

Dimethylformamide → 5-(Benzyloxy)-2-methylpyridine

https://huagongshe.com/reaction/1691221

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 title compound (5.99 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-fa68dbb96bd74f58bcd7242f35c06218
Source noteuspto-grants-2012_04