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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925079Generated: November 2, 2026

Glycolic Acid → 2-(2-Hydroxy-acetyl)-hexahydro-cyclopenta[c]pyrrol-5-one

https://huagongshe.com/reaction/1925079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycolic AcidHCID 757—
ReactantTriethylamineHCID 8471—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHexahydrocyclopenta(c)pyrrol-5(1H)-oneHCID 46911901—
SolventAcetonitrileHCID 6342—
Product2-(2-Hydroxy-acetyl)-hexahydro-cyclopenta[c]pyrrol-5-oneHCID 5915153364%

Reaction Conditions

Temperature25 °C

Reaction Steps

Hexahydro-cyclopenta[c]pyrrol-5-one triflutate 1f (764.8 mg, 3.2 mmol) and 2-hydroxyacetic acid (267.5 mg, 3.52 mmol) were dissolved in 10 mL of acetonitrile, and hydroxyacetic acid (1.3 g, 9.6 mmol), 1-ethyl-3-dimethylaminopropyl-carbodiimide hydrochloride (1.23 g, 6.4 mmol) and triethylamine (1.3 mL, 9.6 mmol) were then added to the solution in an ice-water bath. The ice-water bath was then removed, and the reaction mixture was stirred overnight at 25° C. The solvent was evaporated, and 20 mL of ethyl acetate was then added to the residue. The mixture was filtered and the filtrate was washed with 20 mL of water. The combined organic extracts were 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-(2-hydroxy-acetyl)-hexahydro-cyclopenta[c]pyrrol-5-one 3a (0.375 g, yield 64%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178575B2
Source datasetuspto-grants-2012_05
ORD IDord-4406091749924f2e9255f44ca3709db9
Source noteuspto-grants-2012_05