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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49749Erstellt: 24. Oktober 2026

Water → 3,3'-Diamino-4,4'-di-2-furoylaminobiphenyl

https://huagongshe.com/de/reaction/49749

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAmmonium ChlorideHCID 25517—
EduktIndiumHCID 5359967—
Edukt3,3'-Dinitro-4,4'-di-2-furoylaminobiphenylHCID 22741599—
LösungsmittelEthanolHCID 702—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt3,3'-Diamino-4,4'-di-2-furoylaminobiphenylHCID 2274160223,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Into a separable flask equipped with a stirrer and a reflux condenser cooled with water, 7.4 g of 3,3′-dinitro-4,4′-di-2-furoylaminobiphenyl, 100 ml of N-methyl-2-pyrrolidone and 75 ml of ethyl alcohol were placed. After adding 40 ml of a saturated aqueous solution of ammonium chloride, 25.6 g of powder of indium metal was added to the prepared solution. The obtained mixture was stirred at 80° C. for 1 hour. After the reaction solution was cooled to the room temperature, the solid substance was removed by filtration. The filtrate was concentrated to about one half at a reduced pressure. To the concentrated filtrate, 300 ml of water was added and the formed solid substance was separated by filtration to obtain 2.9 g of a crude product. The crude product was purified in accordance with the silica gel column chromatography to obtain 1.5 g of 3,3′-diamino-4,4′-di-2-furoylaminobiphenyl. The yield of the isolated product was 23%. This product was recrystallized from N-methyl-2-pyrrolidone/ethyl acetate (the volume ratio: 25/75) and needle crystals having a decomposition temperature of 256 to 259° C. were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06709804B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-70a34d2cf4ca4b2c893e159113b9d888
Quellennotizuspto-grants-2004_03