HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912399Generated: November 1, 2026
Bromobenzene → Piperazine, 1-methyl-4-phenyl-
https://huagongshe.com/reaction/912399
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | Piperazine, 1-methyl-4-phenyl- | HCID 200991 | 74.4% |
Reaction Steps
A 1 L flask was charged with 141.3 g of bromobenzene, 30.1 g of 1-methylpiperazine and 43.8 g of potassium tert-butoxide. The flask was then placed on an ice bath for 10 minutes and the contents rapidly stirred. 2.04 g of “PEPPSI” catalyst[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)-palladium (II) dichloride was then added and the flask fitted with a reflux condenser. The reaction was refluxed under a nitrogen atmosphere for 2 hours and then cooled to room temperature. The reaction mixture was then filtered through a pad of 800 mL of silica gel in a 2 L D-filter flask and the pad subsequently rinsed with 600 mL of ether. Then the product was extracted from the pad with ethanol. Evaporation of the ethanol gave 39.4 g of 1-methyl-4-phenylpiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08025863B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-b3f6546dccf24fc48cf06ac33f43e005 |
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| Source note | uspto-grants-2011_09 |
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