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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378363Generated: October 30, 2026

Dimethylformamide → Methyl 2-((4,6-Dimethoxypyrimidin-2-yl)oxy)-3-phenoxy-3-phenylbutanoate

https://huagongshe.com/reaction/378363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dimethoxy-2-(methylsulfonyl)pyrimidineHCID 838363—
ReactantMethyl 3-benzyloxy-3-phenyl-2-hydroxybutyrateHCID 15292268—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductMethyl 2-((4,6-Dimethoxypyrimidin-2-yl)oxy)-3-phenoxy-3-phenylbutanoateHCID 1576682524.5%

Reaction Steps

4.4 g (15.4 mmol) of methyl 3-phenoxy-3-phenyl-2-hydroxybutyrate (Compound 1.1) are dissolved in 40 mol of DMF, and 0.46 g (18.4 mmol) of sodium hydride is added. The mixture is stirred for 1 hour and then 3.4 g (15.4 mmol) of 4,6-dimethoxy-2-methylsulfonylpyrimidine are added. The mixture is stirred at room temperature for 24 hours and then cautiously hydrolyzed with 10 mo of water, the pH is adjusted to 5 with acetic acid, and the solvent is removed by distillation under high vacuum. The residue is taken up in 100 mo of ethyl acetate, washed with water, dried over sodium sulfate and distilled to remove solvents. 10 ml of methyl t-butyl ether are added to the residue, and the precipitate is filtered off with suction. Drying results in 1.6 g of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030975
Source datasetuspto-grants-2000_02
ORD IDord-ecdb800dff944e338678eaef41724959
Source noteuspto-grants-2000_02