HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260415Generated: October 30, 2026
Formic Acid → N-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamide
https://huagongshe.com/reaction/2260415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | L-Aspartic Acid | HCID 5960 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Product | N-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamide | HCID 11298025 | — |
Reaction Steps
0.12 grams (0.003 mole) of magnesium oxide, a catalyst, was dissolved in 16 milliliters (ml) (0.405 mole) of 95% formic acid. 60.2 ml of acetic anhydride was then added to the aforementioned solution which was heated to 35°-40° C. for 10-15 minutes. Subsequently, 39.93 grams (0.3 mole) of L-aspartic acid was added and this mixture was stirred for 2.5 hours at 50°±2° C. At this point, an additional 8.6 ml of acetic anhydride was added and the reaction continued for an additional 2.5 hours at 50±2° C. 9.2 ml (0.120 mole) of isopropyl alcohol was then added to the reaction mixture and heating was continued for an additional two hours. N-formyl aspartic anhydride was formed at this point as shown by high performance liquid chromatography (HPLC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05476961 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-21551c9365a844a0991910e7b4452253 |
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| Source note | uspto-grants-1995_12 |
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