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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297045Generated: October 30, 2026

Water → Tert-butyl 2-(3-pyridyloxy)acetate

https://huagongshe.com/reaction/1297045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-HydroxypyridineHCID 7971—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-(3-pyridyloxy)acetateHCID 2266805332.5%

Reaction Steps

To a suspension of 0.22 g of sodium hydride (60% oil dispersion, 5.5 mmol) in 2 mL of DMF was added dropwise a solution of 0.48 g of 3-hydroxypyridine (5.0 mmol) in 2 mL of DMF at room temperature, and the mixture was stirred for an hour. The resulting brown solution was ice-cooled, 0.81 mL of tert-butyl bromoacetate (5.5 mmol) was added, and the mixture was stirred under ice-cooling for an hour followed by stirring at room temperature for 2 hours. After addition of water, the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried and evaporated. The residue was purified by column chromatography on silica gel (eluent: chloroform:ethyl acetate=5:1), to give 0.34 g of tert-butyl 3-pyridyloxyacetate (Yield: 32.5%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039754E1
Source datasetuspto-grants-2007_07
ORD IDord-ada4cb52959642e394324c1f71868e10
Source noteuspto-grants-2007_07