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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267841Generated: November 1, 2026

Ammonium Hydroxide → 6,6'-Bis(phenylethynyl)[1,1'-biphenyl]-3,3',4,4'-tetramine

https://huagongshe.com/reaction/267841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 21554339HCID 21554339—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product6,6'-Bis(phenylethynyl)[1,1'-biphenyl]-3,3',4,4'-tetramineHCID 2262529976%

Reaction Steps

A solution of 2,2'-bis(phenylethynyl)-5,5'-dinitrobenzidine (0.474 g, 0.00100 mol) in dioxane (50 ml), freshly distilled from FeSO4 (3.65 g, 0.024 mol), was added to a boiling solution of FeSO4 (3.65 g, 0.024 mol) in water (50 ml.) which was stirred under nitrogen. After 5 minutes, ammonium hydroxide (20 ml, 30%) was added slowly followed by 20 ml. more of dioxane. The resultant dark suspension was stirred and refluxed for 30 minutes at which point additional ammonium hydroxide (20 ml) was added. Refluxing was continued for 30 minutes and then the reaction mixture was cooled and extracted three times with 100 ml. of chloroform. The combined chloroform extracts were concentrated to dryness on a rotary evaporator. The residue was dissolved in methylene chloride (20 ml.) and filtered after which the filtrate was poured with stirring into 20 ml. of hexane. The resultant precipitate was filtered, washed with hexane, and dried at 23° C in a vacuum oven at 1 mm of Hg for 24 hours to give 0.313 g (76% yield) of 2,2'-bis(phenylethynyl)-5,5'-diaminobenzidine which softened above 100° C to a viscous melt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03944614
Source datasetuspto-grants-1976_03
ORD IDord-450e3532781e4938a2fc4e14e3d7e875
Source noteuspto-grants-1976_03