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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352226Generated: October 26, 2026

Sodium hydride → Pyridin-3-yl-(pyridin-2-yloxy)-acetic acid ethyl ester

https://huagongshe.com/reaction/352226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-bromo-2-(pyridin-3-yl)acetateHCID 21985933—
ReactantHCID 178516071HCID 178516071—
SolventDimethylformamideHCID 6228—
ProductPyridin-3-yl-(pyridin-2-yloxy)-acetic acid ethyl esterHCID 698489053%

Reaction Steps

Sodium hydride (520 mg; 21.8 mmol; 1.4 equiv) was stirred with 2-hydroxypyridine (1.73 g; 18.2 mmol; 1.2 equiv) in DMF (30 mL) for 15 min. This solution was added to an aliquot of bromo-pyridin-3-yl-acetic acid ethyl ester (approx. 3.6 g; 15 mmol) in DMF (20 mL). After stirring overnight, at rt., the resulting opaque black solution was concentrated in vacuo, dissolved in 20% isopropyl alcohol/chloroform, washed 5 times with saturated NaHCO3(aq), washed twice with saturated NaCl(aq), and dried over Na2SO4(s). After filtration, the solution was concentrated in vacuo and purified by SiO2 column chromatography on two consecutive columns with a 1% methanol/chloroform mobile phase and then an ethyl acetate/hexanes mobile phase (30%, 40%, 50% step gradient). A light yellow oil (134 mg; approx. 3% yield) was isolated. MS(ES) calc'd: [M+H]+=259.2 m/z. Found: 259.1 m/z.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743794B2
Source datasetuspto-grants-2004_06
ORD IDord-d94fa65d735a4eb0a54115991fc4408a
Source noteuspto-grants-2004_06