関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Furfurylamine | HCID 3438 | — |
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Malononitrile | HCID 8010 | — |
| 反応物 | Furoin | HCID 11100 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-Amino-1-(2-furanylmethyl)-4,5-difuryl-3-pyrrolecarbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05925152 |
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| 出典データセット | uspto-grants-1999_07 |
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| ORD ID | ord-a1ff9dcd14714eac927c69bd9159b305 |
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| 出典メモ | uspto-grants-1999_07 |
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