HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070517Generated: October 25, 2026
Ethyl Glycolate → Ethyl 2-pyrimidinyloxyacetate
https://huagongshe.com/reaction/1070517
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Glycolate | HCID 12184 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-pyrimidinyloxyacetate | HCID 22396258 | 77.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903085B1 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-7a6f9565a97145d29f1adc35a6d34fb6 |
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| Source note | uspto-grants-2005_06 |
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