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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601728Generated: October 26, 2026

Triethylamine → Etiracetam, (R)-

https://huagongshe.com/reaction/601728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(2-Oxopyrrolidin-1-yl)butanoic acid, (2R)-HCID 11600747—
SolventDichloromethaneHCID 6344—
ProductEtiracetam, (R)-HCID 44134180.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of (R)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (35 g, 0.20 mol) in methylene chloride (225 ml) was cooled to 0° C. and triethylamine (41 g, 0.40 mol) and methanesulfonyl chloride (29 g, 0.26 mol) were added dropwise. The mixture was stirred at 0° C. for 30 min., then a stream of ammonia was purged in the solution at 0° C. for 2 hours. The insoluble solids were filtered and the filtrate was concentrated. The product was recrystallized from methyl isobutyl ketone to give 27.5 g (78%) of (R)-alpha-ethyl-2-oxo-1-pyrrolidineacetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902380B2
Source datasetuspto-grants-2011_03
ORD IDord-fe3d671ac3dd48b7a8e1e125bcf09ad2
Source noteuspto-grants-2011_03