HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390002Generated: October 28, 2026
Piperazine → 1-(4-tert-Butylphenyl)piperazine
https://huagongshe.com/reaction/390002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 1-Bromo-4-tert-butylbenzene | HCID 77595 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | HCID 178424406 | HCID 178424406 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-tert-Butylphenyl)piperazine | HCID 781722 | 48.2% |
Reaction Steps
1-Bromo-4-t-butylbenzene (2.38 mL, 14 mmol), piperazine (1.8 g, 21 mmol), sodium t-butoxide (1.95 g, 20.3 mmol) and dichlorobis(tri-o-tolylphosphine)palladium(II) (330.1 mg, 0.42 mmol) were dissolved in anhydrous toluene and reacted for 3 hours while heating at 100° C. After identifying complete disappearance of 1-bromo-4-t-butylbenzene by TLC, the reaction solution was filtered with celite. The filtrate was concentrated and purified by separation through column chromatography (CH2Cl2/MeOH, 1:1). A target compound (1.47 g, 6.732 mmol, 48.2%) was yielded.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383631B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d5a2f9ca450d48f7a7094e272f63522c |
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| Source note | uspto-grants-2013_02 |
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