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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925084Generated: November 2, 2026

Citric Acid → 2-(Pyrrolidine-1-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-one

https://huagongshe.com/reaction/1925084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTriethylamineHCID 8471—
Reactant1-Pyrrolidinecarbonyl chlorideHCID 70937—
ReactantHexahydrocyclopenta(c)pyrrol-5(1H)-oneHCID 46911901—
SolventDichloromethaneHCID 6344—
Product2-(Pyrrolidine-1-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-oneHCID 5915152358.5%

Reaction Steps

Hexahydro-cyclopenta[c]pyrrol-5-one triflutate 1f (478 mg, 2 mmol) was dissolved in 20 mL dichloromethane, and pyrrolidine-1-carbonyl chloride (0.276 mL, 2.5 mmol) and triethylamine (0.84 mL, 6 mmol) were then added to the solution in an ice-water bath. Upon completion of the addition, the reaction mixture was stirred overnight at room temperature, 10% citric acid solution was then added to the mixture to adjust to pH 4. The mixture was extracted with dichloromethane (50 mL×3). The combined organic extracts were washed with 50 mL of saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 2-(pyrrolidine-1-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-one 8a (0.26 g, yield 58.5%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178575B2
Source datasetuspto-grants-2012_05
ORD IDord-75fbdeaf84df46299324d70ebe6fbc01
Source noteuspto-grants-2012_05