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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
Reactant2,5-Bis{4-[2-(4-nitrophenyl)ethenyl]phenyl}-1,3,4-oxadiazoleHCID 53888135—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product2,5-Bis[4-(p-aminostyryl)phenyl]-1,3,4-oxadiazoleHCID 5433972794.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251613
Source datasetuspto-grants-1981_02
ORD IDord-230eca3e06854635ae84eacd4b7c9e6b
Source noteuspto-grants-1981_02