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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112355Generated: October 31, 2026

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

https://huagongshe.com/reaction/2112355

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) is 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 numberUSRE040703E1
Source datasetuspto-grants-2009_04
ORD IDord-95e10a36cbf44820a7cbecf8f2ad9346
Source noteuspto-grants-2009_04