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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416583Generated: October 31, 2026

Hydrochloric Acid → HCID 68829902, compound

https://huagongshe.com/reaction/2416583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-(diethoxyphosphorylmethyl)benzoateHCID 10946061—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 68829902HCID 68829902—

Reaction Steps

4.80 g (16.8 mmol) of methyl 4-(diethoxyphosphorylmethyl)benzoate was dissolved in 100 ml of tetrahydrofuran. 620 mg (15.5 mmol) of sodium hydride was added to the obtained solution under cooling with ice, and the obtained mixture was stirred for 30 minutes and then stirred at room temperature for additional 30 minutes. 1.38 g (12.9 mmol) of pyridine-4-aldehyde was added to the mixture, and they were stirred for 20 hours. After the treatment with ethyl acetate as the extraction solvent in an ordinary manner, the obtained crude product was dissolved in 30 ml of methanol. 300 mg of 10% palladium-carbon was added to the obtained solution, and they were stirred in the presence of hydrogen for 20 hours. After the filtration through Celite, the solvent was evaporated. The residue was dissolved in 30 mol of concentrated hydrochloric acid, and the obtained solution was stirred at 40° C. overnight. The solvent was evaporated to obtain the crude title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825181B1
Source datasetuspto-grants-2004_11
ORD IDord-6fadedcb910340749af7dc54e8e74824
Source noteuspto-grants-2004_11