HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256364Generated: October 25, 2026
Triethylamine → 2,2-Dimethyl-5-oxo-3-(2-oxo-1-pyrrolidineacetyl)-1-imidazolidineacetamide
https://huagongshe.com/reaction/256364
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butyl chloroformate | HCID 61140 | — |
| Reactant | 2-(2-Oxopyrrolidin-1-yl)acetic acid | HCID 3146687 | — |
| Reactant | 2,2-Dimethyl-5-oxo-1-imidazolidineacetamide | HCID 20155466 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,2-Dimethyl-5-oxo-3-(2-oxo-1-pyrrolidineacetyl)-1-imidazolidineacetamide | HCID 20163709 | — |
Reaction Steps
An ice cold solution of 2-oxo-1-pyrrolidineacetic acid (1.45 g) and triethylamine (1.45 ml) in dimethylformamide (7 ml) was treated dropwise while stirring with butyl chloroformate (1.3 ml). After stirring at 0° C. for 45 minutes, 2,2-dimethyl-5-oxo-1-imidazolidineacetamide (1.75 g) was added at once and stirring was prolonged at room temperature overnight. After evaporation under reduced pressure, the residue was chromatographed on a silica gel column, eluting with dichloromethane/methanol 1:1. The selected fractions were collected and evaporated, the residue was taken up with ethyl acetate and the resulting solid was crystallized from ethanol, to give the title compound as a white powder, m.p. 225°-227° C., (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04703054 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-8bd97c6e19a4404ca2ced4eba6826bdc |
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| Source note | uspto-grants-1987_10 |
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