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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075286Generated: October 31, 2026

Alpha-Aminobutyric Acid → HCID 178437617, compound

https://huagongshe.com/reaction/1075286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAlpha-Aminobutyric AcidHCID 6657—
ReactantHCID 178468373HCID 178468373—
SolventAcetonitrileHCID 6342—
ProductHCID 178437617HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395547
Source datasetuspto-grants-1983_07
ORD IDord-273f0ddda51d4d05bf02b908414aa2a1
Source noteuspto-grants-1983_07