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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826583Generated: November 1, 2026

1-Boc-4-(4-Nitrophenyl)piperazine → tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1826583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(4-Nitrophenyl)piperazineHCID 3380696—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 1101130197%

Reaction Steps

To a suspension of 1.46 g (4.8 mmol) of 4-(4-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl ester (Example 11) and 1 g of Raney Nickel in 50 mL of tetrahydrofuran is added hydrogen to an initial pressure of 54.5 psi. The reaction is shaken for 14 hours and then filtered. The filtrate is concentrated to give 1.29 g (97%) of the product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053070B2
Source datasetuspto-grants-2006_05
ORD IDord-03cb6d1798b04518a5fba4a8b19b7f82
Source noteuspto-grants-2006_05