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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164865Generated: October 31, 2026

Tetraethyl methylenediphosphonate → HCID 86743785, compound

https://huagongshe.com/reaction/1164865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethyl methylenediphosphonateHCID 15455—
ReactantHCID 15618374HCID 15618374—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86743785HCID 86743785—

Reaction Steps

A stirred solution of 5.3 ml of bis-(diethylphosphono)methane in 30 ml of anhydrous tetrahydrofuran (THF) under nitrogen is cooled to -78° and 8.5 ml of 2.5M butyl lithium is added dropwise. After stirring 5 minutes a solution of 4.64 g of ethyl 1-ethoxycarbonyl-3-oxo-pyrrolidine-2-carboxylate [J. Am. Chem. Soc. 86, 5297 (1964)] in 30 ml dry THF is added dropwise rapidly. The solution is heated at reflux for 18 hours, cooled to room temperature and concentrated; 40 ml of 1N hydrochloric acid is added and the mixture is extracted with 100 ml of methylene chloride. The organic fraction is washed with 25 ml water, dried over Na2SO4, filtered and concentrated. Purification by flash chromatography using ethyl acetate as solvent yields ethyl 1-ethoxycarbonyl-3-(diethylphosphonomethyl-2,5-dihydropyrrole-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906621
Source datasetuspto-grants-1990_03
ORD IDord-9803335cad6e473e9fba1fce23d4d1d2
Source noteuspto-grants-1990_03