Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070517Generated: October 25, 2026

Ethyl Glycolate → Ethyl 2-pyrimidinyloxyacetate

https://huagongshe.com/reaction/1070517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl GlycolateHCID 12184—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-ChloropyrimidineHCID 74404—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-pyrimidinyloxyacetateHCID 2239625877.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl glycolate (1.04 g) was dissolved in tetrahydrofuran (10 ml) and the solution was cooled to 0° C. Sodium hydride (60% suspension in oil, 0.43 g) was added and the suspension was stirred and then sonicated in an ultrasonic bath. 2-Chloropyrimidine (1.14 g) was added and the mixture was sonicated for a further 110 min. Ammonium chloride solution was added and the mixture was extracted thrice with ethyl acetate, the organic phases were washed with brine and dried, filtered and evaporated. The residue was purified by chromatography eluting with iso-hexane:ethyl acetate (13:7) to give the subtitle compound (1.40 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903085B1
Source datasetuspto-grants-2005_06
ORD IDord-7a6f9565a97145d29f1adc35a6d34fb6
Source noteuspto-grants-2005_06