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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407631Generated: November 2, 2026

Acetic Anhydride → Lacosamide

https://huagongshe.com/reaction/2407631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant(R)-2-Amino-N-benzyl-3-methoxypropionamideHCID 10104501—
ProductLacosamideHCID 219078—

Reaction Steps

The (R)-2-amino-N-benzyl-3-methoxypropionamide solution prepared above was cooled to <5° C. and acetic anhydride (10 ml, 0.106 mol) added at <15° C. The reaction mixture is warmed to room temperature over 30 minutes and aged for a further 30 minutes. The mixture is then washed with water (44 ml), 8% sodium bicarbonate (44 ml) and water (44 ml). The methylene chloride was exchanged for ethyl acetate by distillation and the solution distilled to a volume of 115 ml. The product was crystallised by cooling the solution to 0-5° C. and the pure Lacosamide isolated by filtration (18.7 g, 69.8%) HPLC purity 99.98%, Chiral purity 99.8% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809585B2
Source datasetuspto-grants-2014_08
ORD IDord-bcd706ee98ee478aa60cc25ea5ac4654
Source noteuspto-grants-2014_08