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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 582439생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물FurfurylamineHCID 3438—
반응물p-Toluenesulfonic acidHCID 6101—
반응물MalononitrileHCID 8010—
반응물FuroinHCID 11100—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물2-Amino-1-(2-furanylmethyl)-4,5-difuryl-3-pyrrolecarbonitrileHCID 23217605—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05925152
출처 데이터셋uspto-grants-1999_07
ORD IDord-a1ff9dcd14714eac927c69bd9159b305
출처 메모uspto-grants-1999_07