Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (+-)-HCID 11126541—
Reactant1-(2-Aminoacetyl)-2,2-dimethyl-4-imidazolidinoneHCID 20163713—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,2-Dimethyl-1-[2-(4-hydroxy-2-oxo-1-pyrrolidineacetamido)acetyl]-4-imidazolidinoneHCID 5443508721.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04703054
Source datasetuspto-grants-1987_10
ORD IDord-3c6d88fb788c483799df28de6c388000
Source noteuspto-grants-1987_10