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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-nitrotolueneHCID 82189—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product4-(2-Methyl-5-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 66599900—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183237B2
Source datasetuspto-grants-2012_05
ORD IDord-c48c4773b233401eb1e2513e59c0eadd
Source noteuspto-grants-2012_05