HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345331Generated: October 28, 2026
Tetraethyl methylenediphosphonate → HCID 14850767, compound
https://huagongshe.com/reaction/345331
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 14850767 | HCID 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-(diethylphosphonomethyl)-2,5-dihydropyrrole-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057506 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-77a6cf10847c449b9d2fe7f891e9ffd9 |
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| Source note | uspto-grants-1991_10 |
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