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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865923Generated: October 31, 2026

Phosphoric Acid → HCID 15279442, compound

https://huagongshe.com/reaction/865923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dimethoxy-2-(methylsulfonyl)pyrimidineHCID 838363—
ReactantHCID 15279441HCID 15279441—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 15279442HCID 1527944217.2%

Reaction Steps

2.0 g of 2,2,2-trifluoroethanol are introduced into 80 ml of dimethylformamide and 0.60 g of 80% strength sodium hydride is added at room temperature. After 1 h, a clear solution has formed and 5.0 g of 2,2-dimethyl-5-trimethylsilylethynyl-4H-(1,3)benzodioxin-4-one are added at room temperature. After 20 min, 4.0 g of 4,6-dimethoxy-2-methylsulfonylpyrimidine are added and the reaction solution is stirred overnight at room temperature. It is then poured into 400 ml of water containing phosphoric acid (pH 3) at 0° C. and extracted with methyl tert-butyl ether, and the combined organic phases are washed with water, dried over sodium sulfate and concentrated. 6.4 g of crude product remain, which is chromatographed on silica gel using n-hexane/ethyl acetate. A colorless oil (1.2 g) is obtained. 1H-NMR (CDCl3): δ=3.33 (s); 3.83 (s); 4.55 (q); 5.80 (s); 7.25-7.50 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569640
Source datasetuspto-grants-1996_10
ORD IDord-873fb7613cb44736ab124d3d3130b8eb
Source noteuspto-grants-1996_10