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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709042Generated: October 30, 2026

Formic Acid → N-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamide

https://huagongshe.com/reaction/1709042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantL-Aspartic AcidHCID 5960—
ReactantAcetic AnhydrideHCID 7918—
ReactantMagnesium monoxideHCID 6850729—
ProductN-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamideHCID 11298025—

Reaction Steps

Magnesium oxide (0.121 grams; 0.003 mole) was dissolved in 19.3 grams (0.4 mole) of 95% formic acid under nitrogen. Acetic anhydride (69.3 grams; 0.655 mole) was then added to the solution which was stirred for 10-15 minutes. The temperature of the mixture rose to 40° C. L-aspartic acid (39.93 grams; 0.30 mole) was added to the mixture and the resulting slurry was stirred at about 50° C. for about 6 hours. N-formyl-L-aspartic anhydride was formed at this point as shown by high performance liquid chromatography (HPLC). The mixture was then filtered and washed with 30 grams of acetic acid in order to isolate the N-formyl-L-aspartic anhydride. The yield of the N-formyl-L-aspartic anhydride from the L-aspartic acid was 80%. The N-formyl-L-aspartic anhydride will include some acetic acid, which remains for use as a solvent in the coupling step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946988
Source datasetuspto-grants-1990_08
ORD IDord-3b5dbfe063f64c5b8c721609f736b720
Source noteuspto-grants-1990_08