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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198888Generated: November 3, 2026

Tetraethyl methylenediphosphonate → HCID 14850767, compound

https://huagongshe.com/reaction/1198888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethyl methylenediphosphonateHCID 15455—
ReactantHCID 15618374HCID 15618374—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14850767HCID 14850767—

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-oxopyrrolidine-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-(diethylphosphono- methyl)-2,5-dihydropyrrole-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898854
Source datasetuspto-grants-1990_02
ORD IDord-eaaae27c94ed4ba28cf7fd3f1418ba1f
Source noteuspto-grants-1990_02