HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261378Generated: November 3, 2026
Acetic Acid → 3-Pyrrolidineacetamide, N-hydroxy-2-oxo-1-(phenylmethyl)-
https://huagongshe.com/reaction/2261378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl [2-oxo-1-(2-phenylethyl)pyrrolidin-3-yl]acetate | HCID 21750807 | — |
| Reactant | HCID 178514655 | HCID 178514655 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | 3-Pyrrolidineacetamide, N-hydroxy-2-oxo-1-(phenylmethyl)- | HCID 11265146 | 14% |
Reaction Steps
12 mg of (2-oxo-1-phenethyl-pyrrolidin-3-yl)-acetic acid methyl ester (25r) prepared by the above Step 1 was dissolved in methanol solution (0.04 mmol) and then 1.7 M methanolic suspension solution containing NH2OK (0.07 ml, 0.12 mmol) was added thereto at 0° C. and the resulting mixture was stirred for 4 hrs at room temperature. The resulting mixture was neutralized with 0.02 ml of acetic acid, diluted with 10% methanol/chloroform solution, filtered and concentrated in vacuo. The resulting compound was purified by Silica gel column chromatography with a solvent mixture mixed with methanol and chloroform (1:9) as an eluant to give 1.6 mg of 2-(1-benzyl-2-oxo-pyrrolidin-3-yl)-N-hydroxy-acetamide (25s) (yield: 8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846963B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-86ec883440e04f789e7bc776cd791364 |
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| Source note | uspto-grants-2010_12 |
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