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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886300Generated: October 25, 2026

Dimethylformamide → Ethyl 2-(4,6-dimethylpyrimidin-2-yl)oxyacetate

https://huagongshe.com/reaction/1886300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl GlycolateHCID 12184—
Reactant4,6-Dimethyl-2-methylsulfonylpyrimidineHCID 2772382—
SolventWaterHCID 962—
ProductEthyl 2-(4,6-dimethylpyrimidin-2-yl)oxyacetateHCID 3410252—

Reaction Steps

A solution containing 4,6-dimethyl-2-methylsulfonylpyrimidine (10.0 g, 53.8 mmol), ethyl glycolate (5.60 g, 53.8 mmol), and 30 mL of N,N -dimethylformamide was prepared and to this was added with stirring potassium carbonate (8.0 g, 60 mmol). The mixture was allowed to stir at ambient temperature overnight. It was then poured into water and the resulting mixture was extracted 3 times with ethyl acetate. The combined organic extracts were extracted with water. The aqueous extract was saturated with sodium chloride and extracted twice more with ethyl acetate. All of the ethyl acetate layers were combined, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 8.20 g (72.6 percent of theory) of the title compound as a yellow oil. This oil was filtration chromatographed on silica gel, eluting with a 30:70 mixture of ethyl acetate and hexane. The product containing eluate was concentrated by evaporation under reduced pressure to obtain 7.9 g (70 percent of theory) of the title compound as a colorless oil which solidified on standing to a white solid melting at 57°-59° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151113
Source datasetuspto-grants-1992_09
ORD IDord-d3d9b63ea6e449bc91fb52632da38ab6
Source noteuspto-grants-1992_09