HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087817Generated: November 2, 2026
1-Phenylpiperazine → HCID 14763436, compound
https://huagongshe.com/reaction/1087817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14763436 | HCID 14763436 | 57.4% |
Reaction Steps
To a solution of 5.7 g (0.035 mole) of 1,1'-carbonyldiimidazole in 75 ml of tetrahydrofuran (THF) was added a solution of 3.5 g (0.034 mole) of 3-dimethylaminopropylamine in 75 ml of THF and the reaction mixture was stirred at ambient temperature for 1.5 hr. A solution of 4.9 g (0.03 mole) of 1-phenylpiperazine in 50 ml of THF was added and the reaction mixture was heated at reflux for 20 hr. The solution was concentrated under reduced pressure and the residue was dissolved in 150 ml of benzene. The solution was washed thrice with 50 ml portions of water and once with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give an oil as residue which crystallized upon standing. The solid was triturated with petroleum ether (30°-60° C.), collected by filtration and recrystallized from cyclohexane to yield 5.0 g (57%) of title compound as a white solid, m.p. 91°-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04960776 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-66521629da094bd5bd639b17f0090c09 |
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| Source note | uspto-grants-1990_10 |
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