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HRID 1906166作成日:2026年10月25日

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

https://huagongshe.com/reaction/1906166

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Butanedione, 1-(2-furanyl)-HCID 12168—
反応物Ammonium AcetateHCID 517165—
溶媒TolueneHCID 1140—
生成物3-Amino-1-(2-furanyl)-2-buten-1-oneHCID 7044814548.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04650806
出典データセットuspto-grants-1987_03
ORD IDord-1c1a73a4389c4affa6a806ad68320814
出典メモuspto-grants-1987_03