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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285365Generated: October 26, 2026

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

https://huagongshe.com/reaction/1285365

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 numberUS04567186
Source datasetuspto-grants-1986_01
ORD IDord-1209be109e7249fea50eda207f6951dc
Source noteuspto-grants-1986_01