HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452323Generated: October 31, 2026
1-(2-Methoxyphenyl)piperazine → HCID 24835288, compound
https://huagongshe.com/reaction/1452323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19972458 | HCID 19972458 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 24835288 | HCID 24835288 | 78.4% |
Reaction Steps
A mixture of 3.56 g of Intermediate XV, 2.35 g of 1-(2-methoxyphenyl)-piperazine, 2.76 g of anhydrous potassium carbonate and 1.66 g of potassium iodide in 25 ml of dimethylformamide was stirred at 100° C. for 6 hours. After cooling, the solvent was removed in vacuo and the residue was taken up in 50 ml of water, stirred for 1 hour at room temperature, collected by filtration, washed with water and crystallized from 95% ethanol in the presence of a small amount of activated charcoal (for decoloring). The base was dissolved in 105 ml of boiling 0.086N aqueous hydrochloric acid solution. After cooling, the crystallized salt was collected by filtration, giving 4.3 g of the title compound (m.p. 201°-203° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05605896 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-48394c5d676d4339bf3e27e63f9fd4cc |
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| Source note | uspto-grants-1997_02 |
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