HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459870Generated: October 30, 2026
Hydrochloric Acid → HCID 18444273, compound
https://huagongshe.com/reaction/459870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18444282 | HCID 18444282 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18444273 | HCID 18444273 | 12.5% |
Reaction Steps
To 297 mg of 4-[6-(3,4-dimethoxyphenyl)pyridine-2-carbonyl]-1-(4-hydroxyphenyl)piperazine were added 623 mg of [1,3]dioxolan-2-one and 147 mg of potassium carbonate, followed by 1.5 hours of stirring at 100° C. After the mixture was cooled to room temperature, water and then 1M hydrochloric acid were added to the reaction solution, which was then neutralized with a saturated aqueous sodium hydrogen carbonate solution, followed by extraction with chloroform. The organic layer was washed with brine and then dried over anhydrous magnesium sulfate, and thereafter, the solvent was evaporated. The residue was purified by silica gel column chromatography (chloroform-methanol) and then recrystallization was carried out from ethyl acetate to obtain 41 mg of 2-(4-{4-[6-(3,4-dimethoxyphenyl)pyridine-2-carbonyl]piperazin-1-yl}phenoxy)ethanol as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07196080B2 |
|---|
| Source dataset | uspto-grants-2007_03 |
|---|
| ORD ID | ord-25e6f87c24794dfcbfc45201e58915d2 |
|---|
| Source note | uspto-grants-2007_03 |
|---|