Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49749Generated: October 25, 2026

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

https://huagongshe.com/reaction/49749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantIndiumHCID 5359967—
Reactant3,3'-Dinitro-4,4'-di-2-furoylaminobiphenylHCID 22741599—
SolventEthanolHCID 702—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3,3'-Diamino-4,4'-di-2-furoylaminobiphenylHCID 2274160223.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06709804B2
Source datasetuspto-grants-2004_03
ORD IDord-70a34d2cf4ca4b2c893e159113b9d888
Source noteuspto-grants-2004_03