HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638559Generated: October 31, 2026
1-(2-Hydroxyethyl)piperazine → HCID 131714478, compound
https://huagongshe.com/reaction/638559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 20252673 | HCID 20252673 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane ethylacetate | HCID 21226138 | — |
| Solvent | Acetone diethylether | HCID 21584533 | — |
| Product | HCID 131714478 | HCID 131714478 | 55% |
Reaction Steps
A solution of 5.7 g of (5-bromomethylisoxazol-3-yl)-4-fluorophenylmethanone in 100 ml of Et2O was added to a solution of 6.5 g of N-beta-hydroxyethylpiperazine in 400 ml of 25% acetone/Et2O. The resulting mixture was stirred at room temperature for 24 hours. This mixture was filtered and the solution was concentrated in vacuo to give an oil. The residue was dissolved in 300 ml of H2O and shortly thereafter a precipitate formed. The solid was filtered and dried to give 5.2 g of crude solid. A solution of 4.3 g of the amine in 50 ml of 50% ethyl acetate/CH2Cl2 was added dropwise to a solution of excess maleic acid in 600 ml of Et2O. The precipitated salt was filtered and recrystallized from 160 ml of isopropanol to yield 5.2 g (55%) of crystals, m.p. 139°-140°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04562187 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-316db3fcc85c4b198b5e54d65845faa8 |
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| Source note | uspto-grants-1985_12 |
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