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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090286Generated: November 1, 2026

Hydrochloric Acid → HCID 54366659, compound

https://huagongshe.com/reaction/1090286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 54309857HCID 54309857—
CatalystIronHCID 23925—
SolventWaterHCID 962—
ProductHCID 54366659HCID 54366659—

Reaction Conditions

Temperature50 °C

Reaction Steps

11.28 g of the 1,8-bis(4-nitrophenyl)-1,3,5,7-octatetraene synthesized in Synthesis Example 1 was added to 250 ml of DMF. To this mixture, 22.5 g of iron powder was added, and then diluted hydrochloric acid consisting of 5.6 ml of concentrated hydrochloric acid and 19 ml of water was added with stirring. The mixture was further stirred at 80°~88° C. for 5 hours. The reaction mixture was cooled to 50° C. and was made alkaline by addition of a 10% aqueous solution of sodium hydroxide. Celite was added to the reaction mixture, and then insoluble components were filtered out, together with the Celite, from the reaction mixture, while it was hot. The filterate was diluted with water. As a result, crystals separated out. The crystals were filtered off, washed with water and dried, so that a crude diamino product was obtained. The product was recrystallized from a mixed solvent of DMF and water, whereby 1,8-bis(4-aminophenyl)-1,3,5,7-octatetraene was obtained in the form of dark red plate crystals. The melting point was 262.5°~264.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081233
Source datasetuspto-grants-1992_01
ORD IDord-8081e13ea8dc4dd1a621c2d24a200e3b
Source noteuspto-grants-1992_01