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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170405Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 58149524, compound

https://huagongshe.com/reaction/2170405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant2,2-Dimethyl-1-(pyrimidin-5-yl)propan-1-oneHCID 13645650—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58149524HCID 58149524—

Reaction Steps

Under an atmosphere of argon, 10 ml of dimethyl sulphoxide are slowly added dropwise to 0.96 g (4.3 mmol) of trimethylsulphoxonium iodide and 0.17 g of sodium hydride (60%, 4.3 mmol). The reaction mixture is then stirred at room temperature for 15 min, and 0.65 g (3.9 mmol) of 2,2-dimethyl-1-(5-pyrimidinyl)-1-propanone, dissolved in 2 ml of tetrahydrofuran, is added. The reaction mixture is stirred at 50° C. for 90 min. The reaction mixture is then concentrated under reduced pressure, and saturated aqueous sodium chloride solution and ethyl acetate are added to the residue. The organic phase is separated off, dried over sodium sulphate, filtered and concentrated. This gives 0.70 g (99%) of the desired product, which is reacted without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051277B2
Source datasetuspto-grants-2015_06
ORD IDord-07a34458bc71419ea6229dbde16dbb8a
Source noteuspto-grants-2015_06