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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-FluoronitrobenzeneHCID 9590—
Reactant1-BenzylpiperazineHCID 75994—
SolventEthyl AcetateHCID 8857—
Product1-Benzyl-4-(4-nitrophenyl)piperazineHCID 274742747%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960776
Source datasetuspto-grants-1990_10
ORD IDord-eec6965cae1d403eb6c77c281b29249b
Source noteuspto-grants-1990_10