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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 21554339 | HCID 21554339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6,6'-Bis(phenylethynyl)[1,1'-biphenyl]-3,3',4,4'-tetramine | HCID 22625299 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03944614 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-450e3532781e4938a2fc4e14e3d7e875 |
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| Source note | uspto-grants-1976_03 |
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