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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741011Generated: November 2, 2026

Diethyl benzylphosphonate → HCID 14590315, compound

https://huagongshe.com/reaction/1741011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl benzylphosphonateHCID 14122—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Pyridinecarboxaldehyde, 2-amino-HCID 737633—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14590315HCID 1459031540.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

In 35 ml of tetrahydrofuran (THF) was dissolved 1.28 g of 2-aminonicotinaldehyde, followed by addition of 2.50 g of diethyl benzylphosphonate and 2.08 g of potassium hydroxide, and the mixture was refluxed at 80° C. for 4.5 hours. This reaction mixture was filtered to remove insoluble matter and the filtrate was evaporated under reduced pressure. The residue was dissolved in 2N-hydrochloric acid and the solution was washed with ether, made basic bv adding 15% aqueous sodium hydroxide solution, and extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate and the solvent was evaporated off. The residue was recrystallized from acetonitrile to provide 0.83 g of the title compound as yellow prisms. This product was used as a starting material without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972976
Source datasetuspto-grants-1999_10
ORD IDord-87fc2d0942374b7b90b569003d98d873
Source noteuspto-grants-1999_10