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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycolic Acid | HCID 757 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Hexahydrocyclopenta(c)pyrrol-5(1H)-one | HCID 46911901 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(2-Hydroxy-acetyl)-hexahydro-cyclopenta[c]pyrrol-5-one | HCID 59151533 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178575B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-4406091749924f2e9255f44ca3709db9 |
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| Source note | uspto-grants-2012_05 |
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