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HRID 582439作成日:2026年10月24日

Furfurylamine → 2-Amino-1-(2-furanylmethyl)-4,5-difuryl-3-pyrrolecarbonitrile

https://huagongshe.com/ja/reaction/582439

反応式

関与物質

役割名称HCID仕込み量
反応物FurfurylamineHCID 3438—
反応物p-Toluenesulfonic acidHCID 6101—
反応物MalononitrileHCID 8010—
反応物FuroinHCID 11100—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物2-Amino-1-(2-furanylmethyl)-4,5-difuryl-3-pyrrolecarbonitrileHCID 23217605—

反応手順

2-amino-1-(2-furanylmethyl)-4,5-difuryl-3-pyrrolecarbonitrile was prepared as follows: 300 g (1.56 mol) of Furoin (ex Aldrich) was reacted with 151.6 g (1.56 mol) of furfurylamine in the presence of 1.5 g of p-toluenesulphonic acid in toluene under stirring and reflux. The water produced was removed via a Dean Stark trap. When formation of water had ceased (31 ml removed), 103.1 g (1.56 mol) of malononitrile was added as a dispersion in 100 ml toluene, reflux was continued. When again formation of water had ceased (26 ml removed via the Dean Stark trap), the reaction mixture was cooled and the toluene was removed by evaporation. In this way 498 g of a black solid product was obtained. Subsequently, 100 g of this product was purified by flash chromatography (silica, hexane/ethyl acetate as eluant) and 24 g of the product was recovered.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05925152
出典データセットuspto-grants-1999_07
ORD IDord-a1ff9dcd14714eac927c69bd9159b305
出典メモuspto-grants-1999_07