HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926579Generated: November 2, 2026
2-Bromo-4-nitrotoluene → 4-(2-Methyl-5-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1926579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-4-nitrotoluene | HCID 82189 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(2-Methyl-5-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 66599900 | — |
Reaction Steps
In a first flask 0.135 g of palladium acetate (0.135 g, 0.602 mmol) and BINAP (2,2′-bis(diphenylphosphino)-1,1′-binaphthyl) (0.375 g) were suspended in 5 mL of toluene and stirred at 70° C. for 30 min. In a second flask, 2-bromo-1-methyl-4-nitrobenzene (1 g, 4.63 mmol), tert-butyl piperazine-1-carboxylate (1.12 g, 6.02 mmol and sodium tert-butoxide (1.068 g, 11.11 mmol) were added to 5 mL of toluene and stirred for 30 min. at 60° C. To this mixture was added the contents of the first flask, and stirring was continued for 3 h at 60° C. The solvent was evaporated, the residue purified via silica gel chromatography with dichloromethane-methanol (0 to 100%) to yield the title compound (0.145 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183237B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-c48c4773b233401eb1e2513e59c0eadd |
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| Source note | uspto-grants-2012_05 |
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