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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268232Generated: October 25, 2026

Perchloric Acid → Bis (piperazine) p-dihydroxy benzene disulfonate

https://huagongshe.com/reaction/268232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerchloric AcidHCID 24247—
ReactantPiperazine, hexahydrateHCID 120181—
ReactantPotassium PerchlorateHCID 516900—
ReactantPiperazine perchlorateHCID 85529587—
Reactantp-Dihydroxy benzene disulfonic acid potassium saltHCID 131710108—
SolventWaterHCID 962—
ProductBis (piperazine) p-dihydroxy benzene disulfonateHCID 21151652—

Reaction Steps

To an aqueous solution of perchloric acid, containing 200 g of said acid in 500 ml of water 40 % solution, the amount of aqueous solution of piperazine hexahydrate required for neutralization is added. The required amount of piperazine hexahydrate is 388.46 g (C4H10N2.6H2O) dissolved in 500 ml of water. Preferably the pH of the neutralizing solution is controlled to a pH close to 6. The piperazine perchlorate solution is mixed with the warm solution of p-dihydroxy benzene disulfonic acid potassium salt, and is stirred until a copious precipitate of potassium perchlorate is formed, which then increases when the solution is left to cool for several hours. After filtering off the potassium perchlorate, the solution of a piperazine p-dihydroxy benzene disulfonate is concentrated in a rotary evaporator, under vacuum, at 60°C, until crystals begin to form, and it is then left in a refrigerator. The product is filtered and recrystallized in water to give 388 g of bis (piperazine) p-dihydroxy benzene disulfonate, having a melting point of 270°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947448
Source datasetuspto-grants-1976_03
ORD IDord-e3e431b72b86492a8ce5a0f0bb48441c
Source noteuspto-grants-1976_03