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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925081Generated: November 4, 2026

Acetic Anhydride → 2-Acetylhexahydrocyclopenta[c]pyrrol-5(1H)-one

https://huagongshe.com/reaction/1925081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHexahydrocyclopenta(c)pyrrol-5(1H)-oneHCID 46911901—
SolventAcetonitrileHCID 6342—
Product2-Acetylhexahydrocyclopenta[c]pyrrol-5(1H)-oneHCID 1099741872%

Reaction Steps

Hexahydro-cyclopenta[c]pyrrol-5-one triflutate 1f (717 mg, 3 mmol) was dissolved in 20 mL of acetonitrile, and acetic anhydride (0.42 mL, 4.5 mmol) and triethylamine (0.98 mL, 9 mmol) were then added to the solution in an ice-water bath. Upon completion of the addition, the reaction mixture was then stirred overnight in an ice-water bath. The solvent was evaporated, and water (50 mL) was then 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-acetyl-hexahydro-cyclopenta[c]pyrrol-5-one 5a (0.36 g, yield 72%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178575B2
Source datasetuspto-grants-2012_05
ORD IDord-bad541be82e542d9aacba6855f0114a6
Source noteuspto-grants-2012_05