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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982686Generated: November 1, 2026

Ethyl Acetate → HCID 13060175, compound

https://huagongshe.com/reaction/1982686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantOxyselenideHCID 167175—
ReactantHCID 13060169HCID 13060169—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 13060175HCID 13060175—

Reaction Steps

Selenium oxide (9.92 g.) was added to a solution of methyl 2-(2-formamidopyrimidin-4-yl)acetate (14.52 g.) in dioxane (200 ml.) at 90° to 95° C. over 20 minutes, and stirred at the same temperature for an hour. After cooling the resultant solution, the solution was filtered through a column packed with silica gel (20 g.), washed with dioxane and concentrated under reduced pressure. The residue was dissolved in acetone and filtered, and then the filtrate was concentrated under reduced pressure. The residue was triturated with chloroform to give a crude product (8.2 g.). The product was added to ethyl acetate, heated and an insoluble material was filtered out. The filtrate was cooled, and the precipitates were collected by filtration to give methyl 2-(2-formamidopyrimidin-4-yl)glyoxylate (5.55 g.). The product was recrystallized from ethyl acetate (saturated with water) to give mono hydrate thereof, mp 143° to 144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596869
Source datasetuspto-grants-1986_06
ORD IDord-a90dd3d98f70413bac5ab710f7ca4f2c
Source noteuspto-grants-1986_06