HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413922Generated: November 3, 2026
Hydrochloric Acid → 2,5-Bis[4-(p-aminostyryl)phenyl]-1,3,4-oxadiazole
https://huagongshe.com/reaction/1413922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,5-Bis{4-[2-(4-nitrophenyl)ethenyl]phenyl}-1,3,4-oxadiazole | HCID 53888135 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,5-Bis[4-(p-aminostyryl)phenyl]-1,3,4-oxadiazole | HCID 54339727 | 94.3% |
Reaction Steps
After mixing 6.0 g of 2,5-bis[4-(p-nitrostyryl)phenyl]-1,3,4-oxadiazole, 12.0 g of iron powder and 200 g of N,N-dimethyl formamide together, by adding dilute hydrochloric acid prepared by employing 5 ml of undiluted hydrochloric acid and 17 ml of water to the resulting mixture and intensely stirring it, reaction was effected at a temperature of 90° to 100° C. for one hour. After completing the reaction, by adding a 5% aqueous solution of sodium carbonate while heating as above, the pH value of the reactant mixture was adjusted to be 8, the undissolved matter was filtered while heating, and the resulting filtrate was diluted with 70 ml of water, whereby there were separated yellow crystals. Then, said crystals were collected by filtering, washed in water and dried, whereby there were obtained 5.0 g (yield rate: 94.3%) of 2,5-bis[4-(p-aminostyryl)phenyl]-1,3,4-oxadiazole. The melting point of this crystal was 250° C. or more (decomposition point).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04251613 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-230eca3e06854635ae84eacd4b7c9e6b |
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| Source note | uspto-grants-1981_02 |
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