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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37468Generated: October 25, 2026

Phenylphosphonic dichloride → 2-Chloro-3,4-diethoxycarbonyl-5-nitro-6-phenylpyridine

https://huagongshe.com/reaction/37468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylphosphonic dichlorideHCID 69990—
ReactantDiethyl 2-hydroxy-5-nitro-6-phenylpyridine-3,4-dicarboxylateHCID 19935597—
SolventWaterHCID 962—
Product2-Chloro-3,4-diethoxycarbonyl-5-nitro-6-phenylpyridineHCID 19935587—

Reaction Conditions

Temperature150 °C

Reaction Steps

To 1.0 g of 3,4-diethoxycarbonyl-5-nitro-6-phenyl-2-pyridone was added 1.3 ml (3.37 eq.) of phenylphosphonic dichloride, and the mixture was heated at 150° C. for 2.5 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane 1:2), to give an oily product. Yield: 950 mg (90.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420275
Source datasetuspto-grants-1995_05
ORD IDord-c122d6c730f541f4a3dcfbcfd6f66660
Source noteuspto-grants-1995_05