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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250450Generated: November 1, 2026

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

https://huagongshe.com/reaction/2250450

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 numberUS07317028B2
Source datasetuspto-grants-2008_01
ORD IDord-198d41d2827c468783a115f21282074a
Source noteuspto-grants-2008_01