HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164865Generated: October 31, 2026
Tetraethyl methylenediphosphonate → HCID 86743785, compound
https://huagongshe.com/reaction/1164865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetraethyl methylenediphosphonate | HCID 15455 | — |
| Reactant | HCID 15618374 | HCID 15618374 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86743785 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04906621 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-9803335cad6e473e9fba1fce23d4d1d2 |
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| Source note | uspto-grants-1990_03 |
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