HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576299Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 86733975, compound
https://huagongshe.com/reaction/1576299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2,3,4-Trimethoxybenzoic acid | HCID 11308 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 2-(1,4-Diazepan-1-yl)ethan-1-ol | HCID 2736550 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86733975 | HCID 86733975 | 59% |
Reaction Steps
In 150 ml of absolute benzene there were dissolved 1.44 g 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 with ether 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03980643 |
|---|
| Source dataset | uspto-grants-1976_09 |
|---|
| ORD ID | ord-37ffce1bbe6645518976d145165736a8 |
|---|
| Source note | uspto-grants-1976_09 |
|---|