HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087813Generated: October 29, 2026
Hydrochloric Acid → 1-Benzyl-4-(4-nitrophenyl)piperazine
https://huagongshe.com/reaction/1087813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Benzyl-4-(4-nitrophenyl)piperazine | HCID 2747427 | 47% |
Reaction Steps
To 12.5 g (0.07 mole) of methanically stirred 1-benzylpiperazine was added 10.0 g (0.07 mole) of 4-nitrofluorobenzene. After 10 minutes the mixture solidified. The yellow solid was suspended in 50 ml of ethyl acetate and ethereal hydrogen chloride was slowly added to the stirring mixture under a nitrogen atmosphere. The solid was collected (filtration) and partitioned between 10% sodium hydroxide solution and benzene. The benzene layer was washed with ten 100 ml portions of water, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give a yellow oil. Upon cooling, the oil crystallized. The solid was recrystallized from 2-propanol/petroleum ether (60°-110° C.) to give 9.8 g (47%) of yellow solid, m.p. 115°-118° 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-eec6965cae1d403eb6c77c281b29249b |
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| Source note | uspto-grants-1990_10 |
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