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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906166Generated: October 25, 2026

1,3-Butanedione, 1-(2-furanyl)- → 3-Amino-1-(2-furanyl)-2-buten-1-one

https://huagongshe.com/reaction/1906166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Butanedione, 1-(2-furanyl)-HCID 12168—
ReactantAmmonium AcetateHCID 517165—
SolventTolueneHCID 1140—
Product3-Amino-1-(2-furanyl)-2-buten-1-oneHCID 7044814548.9%

Reaction Steps

The intermediate 3-amino-1-(2-furanyl)-2-buten-1-one was prepared as follows: A mixture containing 165 g of 1-(2-furanyl)-1,3-butanedione, 700 ml of toluene and 200 g of ammonium acetate was azeotroped for six hours, cooled and concentrated to dryness in vacuo. The residue was dissolved in isopropyl alcohol, the solution treated with decolorizing charcoal and filtered, and the filtrate concentrated to remove the solvent. The remaining residue was recrystallized from ether-ethanol and dried at room temperature to yield 80.2 g of 3-amino-1-(2-furanyl)-2-buten-1-one, m.p. 128°-130° C. Another 33.4 g of the product, m.p. 128°-130° C. was collected by concentrating the mother liquor and extracting the product with ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04650806
Source datasetuspto-grants-1987_03
ORD IDord-1c1a73a4389c4affa6a806ad68320814
Source noteuspto-grants-1987_03