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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925083Generated: November 1, 2026

Potassium Carbonate → 2-(Morpholine-4-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-one

https://huagongshe.com/reaction/1925083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantHexahydrocyclopenta(c)pyrrol-5(1H)-oneHCID 46911901—
SolventAcetonitrileHCID 6342—
Product2-(Morpholine-4-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-oneHCID 59151512100%

Reaction Steps

Hexahydro-cyclopenta[c]pyrrol-5-one triflutate 1f (574 mg, 2.4 mmol) was dissolved in 20 mL of acetonitrile with stirring, and potassium carbonate (0.397 g, 2.88 mmol) was then added to the solution in an ice-water bath, followed by morpholine-4-carbonyl chloride (0.323 mL, 2.64 mmol). Upon completion of the addition, the reaction mixture was stirred overnight in an ice-water bath, then the solvent was evaporated, and water (50 mL) was added to the residue. The mixture was extracted with ethyl acetate (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-(morpholine-4-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-one 7a (0.572 g, yield 77.3%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178575B2
Source datasetuspto-grants-2012_05
ORD IDord-f5861fdefb8b4d89868acd3e1ae7b696
Source noteuspto-grants-2012_05