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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090818Generated: November 1, 2026

Potassium Carbonate → diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate

https://huagongshe.com/reaction/1090818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriethyl (5-benzoyl-1H-pyrrol-2-yl)methanetricarboxylateHCID 11069430—
CatalystTetrabutylammonium BromideHCID 74236—
Solvent1,2-DichloroethaneHCID 11—
Productdiethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylateHCID 992857480%

Reaction Steps

A mixture of triethyl (5-benzoylpyrrol-2-yl)-methanetricarboxylate (2.00 g, 5 mmol), tetra-butylammonium bromide (1.61 g, 5 mmol) and potassium carbonate (19.0 g, 250 mmol) in 1,2-dichloroethane (100 mL) was refluxed for 2 days. The mixture was cooled to room temperature and filtered. The filter cake was washed with methylene chloride. The filtrate and methylene chloride wash solution were combined and concentrated under reduced pressure. The residue was dissolved in diethyl ether, washed with water, dried, and concentrated. The crude product was purified by flash chromatography on flash silica eluting with hexane/ethyl acetate (90:10) to provide 1.42 g (80%) of diethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylate. The IR and NMR spectral properties were identical to those of the authentic sample.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082950
Source datasetuspto-grants-1992_01
ORD IDord-814ff16ec40e4c6c87c3ce3c4e120972
Source noteuspto-grants-1992_01