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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863460Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 86733975, compound

https://huagongshe.com/reaction/1863460

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,3,4-Trimethoxybenzoic acidHCID 11308—
ReactantMaleic AcidHCID 444266—
Reactant2-(1,4-Diazepan-1-yl)ethan-1-olHCID 2736550—
SolventBenzeneHCID 241—
ProductHCID 86733975HCID 8673397559%

Reaction Steps

In 150 ml of absolute benzene there were dissolved 1.44 of 1-homopiperazineethanol and 9.5 g of p-toluene sulfonic acid. To the resulting solution, 2.75 g of 2,3,4-trimethoxybenzoic acid was added. The system was heated for 16 hours to reflux while removing the formed water. The reaction liquid was cooled, washed with 15% potassium carbonate and then extracted with 10% HCl. After the aqueous layer was washed and then rendered alkaline with potassium carbonate, followed by extraction with ether. After the ethereal layer was dehydrated with a Glauber's salt, the ether was distilled off. The resultant residue was subjected to chromatography using silica gel to obtain a colorless transparent liquid. The liquid was converted into the maleic acid salt thereof in accordance with a conventional manner. Upon recrystallization from ethanol, 1-homopiperazineethanol 2,3,4-trimethoxybenzoate maleate was obtained having a melting point of 112°-113° C. The yield was 59%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04169144
Source datasetuspto-grants-1979_09
ORD IDord-4f518f6f67264fec8b5806ff1c448eaf
Source noteuspto-grants-1979_09