HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256367Generated: October 25, 2026
Dicyclohexylcarbodiimide → 2,2-Dimethyl-1-[2-(4-hydroxy-2-oxo-1-pyrrolidineacetamido)acetyl]-4-imidazolidinone
https://huagongshe.com/reaction/256367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (+-)- | HCID 11126541 | — |
| Reactant | 1-(2-Aminoacetyl)-2,2-dimethyl-4-imidazolidinone | HCID 20163713 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2-Dimethyl-1-[2-(4-hydroxy-2-oxo-1-pyrrolidineacetamido)acetyl]-4-imidazolidinone | HCID 54435087 | 21.9% |
Reaction Steps
Into an ice cold solution of 4-hydroxy-2-oxo-1-pyrrolidineacetic acid (0.95 g) and 1-(2-aminoacetyl)-2,2-dimethyl-4-imidazolidinone (1 g) in dimethylsulfoxide (30 ml) a solution of DCC (1,22 g) in tetrahydrofuran (10 ml) was added dropwise. The solution was stirred at room temperature overnight and then heated at 50° for 4 hours. After cooling the solution was diluted with water and the resulting precipitate was filtered off. The filtrate was evaporated to dryness under vacuum. The residue was dissolved in water and eluted on a column of Amberlite IR 120H (20 ml). The eluate was treated with Amberlite IRA 68 (10 ml), filtered and evaporated under vacuum. The residue was triturated with isopropanol to yield 0.4 g of the title compound, m.p. 227°-229° .
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-3c6d88fb788c483799df28de6c388000 |
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| Source note | uspto-grants-1987_10 |
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