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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256363Generated: October 25, 2026

Triethylamine → 2,2-Dimethyl-1-(2-oxo-1-pyrrolidineacetyl)-4-imidazolidin-one

https://huagongshe.com/reaction/256363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyl chloroformateHCID 61140—
Reactant2-(2-Oxopyrrolidin-1-yl)acetic acidHCID 3146687—
ReactantHCID 21279295HCID 21279295—
SolventDimethylformamideHCID 6228—
Product2,2-Dimethyl-1-(2-oxo-1-pyrrolidineacetyl)-4-imidazolidin-oneHCID 20163719—

Reaction Conditions

Temperature0 °C

Reaction Steps

An ice cold solution of 2-oxo-1-pyrrolidineacetic acid (2.2 g) and triethylamine (2.15 ml) in dimethylformamide (10 ml) was treated dropwise while stirring with butyl chloroformate (1.95 ml). After stirring at 0° C. for 30 minutes, 2,2-dimethyl-4-imidazolidinone (1.75 g) was added at once, and stirring was continued 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 to give an oil which was washed twice with ethyl acetate. The residue was crystallized from ethyl acetate, to give the title compound as a white powder, m.p. 214°-217° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04703054
Source datasetuspto-grants-1987_10
ORD IDord-45569acc942d413f8c9274721a09a574
Source noteuspto-grants-1987_10