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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224147Generated: October 25, 2026

Phosphorus oxychloride → 6-Chloro-1,3-diphenylpyrimidine-2,4-dione

https://huagongshe.com/reaction/2224147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1,3-diphenyl-2,4,6(1H,3H,5H)-pyrimidinetrioneHCID 2784952—
SolventWaterHCID 962—
Product6-Chloro-1,3-diphenylpyrimidine-2,4-dioneHCID 277556374%

Reaction Steps

To 1,3-diphenyl-pyrimidine-2,4,6-trione 19 (78.0 g) obtained in Step 1 was added water (16 ml). Phosphorus oxychloride (422 ml) was added dropwise under stirring at room temperature over 50 min. After the completion of the dropwise addition, the mixture was stirred under heating at 110° C. for 3 hrs. After allowing to cool to room temperature, the reaction mixture was added to ice water by small portions and the mixture was stirred at room temperature and extracted with ethyl acetate. The organic layer was washed with brine and saturated aqueous sodium hydrogen carbonate, and dried over anhydrous sodium sulfate. Anhydrous sodium sulfate was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (hexane:ethyl acetate=2:1→3:2) to give 6-chloro-1,3-diphenyl-1H-pyrimidine-2,4-dione 20 (61.5 g, yield 74%) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378423B2
Source datasetuspto-grants-2008_05
ORD IDord-bdce9818de0d4121ba4a077dc71495df
Source noteuspto-grants-2008_05