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HRID 1285365作成日:2026年10月26日

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

https://huagongshe.com/reaction/1285365

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US04567186
出典データセットuspto-grants-1986_01
ORD IDord-1209be109e7249fea50eda207f6951dc
出典メモuspto-grants-1986_01