HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462219Generated: October 31, 2026
Alpha-Aminobutyric Acid → HCID 178437617, compound
https://huagongshe.com/reaction/1462219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Alpha-Aminobutyric Acid | HCID 6657 | — |
| Reactant | HCID 178468373 | HCID 178468373 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178437617 | HCID 178437617 | — |
Reaction Steps
To 4.78 g (0.037 moles) of 3-oximino-2,4-pentanedione dissolved in 40 ml of acetonitrile was added 3.82 g (0.037 moles) of 2-aminobutyric acid. The mixture was brought to reflux, while stirring rapidly under nitrogen, with an oil bath. After 22.5 h the reaction mixture was cooled, suction filtered, and the residue washed with acetonitrile (50 ml). The combined filtrates were concentrated in vacuo, and the resulting oil dissolved in 1 M hydrochloric acid (30 ml). The acid solution was washed with methylene chloride (4×20 ml), then neutralized with solid potassium carbonate. Extraction with methylene chloride, followed by drying over anhydrous potassium carbonate and concentration in vacuo furnished 0.021 moles (67.8%) yield based on recovered d,l-norvaline) of 5-acetyl-2-ethyl-4-methylimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04459413 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-e17a0184cfbb408881c47f37521b09ee |
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| Source note | uspto-grants-1984_07 |
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