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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072285Generated: October 30, 2026

1-Ethylpiperazine → 1-[2-Hydroxy-3-(4-ethyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-4-ethylpiperazinium hydroxide

https://huagongshe.com/reaction/2072285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-EthylpiperazineHCID 79196—
Reactant3-Hydroxy-2-(phenylamino)-4-(phenylimino)-2-cyclobuten-1-oneHCID 10978329—
Product1-[2-Hydroxy-3-(4-ethyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-4-ethylpiperazinium hydroxideHCID 21407792—

Reaction Steps

A mixture of 4.0 grams of 2-anilino-3-hydroxy-4-(phenylimino)-2-cyclobuten-1-one and 3.4 grams of 1-ethylpiperazine is heated at 194°-198° C. in an atmosphere of dry nitrogen for 30 minutes. The cooled solid is comminuted, washed with anhydrous ethyl ether, and dried and the resulting solid is then extracted with 50 ml. of anhydrous benzene. The benzene solution is treated with activated carbon, filtered, concentrated and cooled. A crystalline solid forms and this is separated by filtration and dissolved in distilled water at room temperature and the solution is filtered and concentrated. A precipitate forms and is separated by filtration to give 1-[2-hydroxy-3-(4-ethyl-1-piperazinyl)-4-oxo-2-cyclobuten-1-ylidene]-4-ethylpiperazinium hydroxide inner salt melting at about 179.5°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04051136
Source datasetuspto-grants-1977_09
ORD IDord-bcf2d8722c2044219b712fbdd28e19d7
Source noteuspto-grants-1977_09