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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43055Generated: October 26, 2026

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

https://huagongshe.com/reaction/43055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(4-Nitrophenyl)piperazineHCID 3380696—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 1101130196.7%

Reaction Steps

A suspension of 4-(4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (Step 8.3) (1.26 g, 4.1 mmol) and palladium on carbon (200 mg) in MeOH (30 mL) was stirred for 30 min at rt, under a hydrogen atmosphere. The reaction mixture was filtered through a pad of celite and concentrated to afford 1.1 g of the title compound as a pink solid: ESI-MS: 278.2 [M+H]+; tR=2.85 min (System 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536175B2
Source datasetuspto-grants-2013_09
ORD IDord-0245bdaea34f4fb5bc1386ff3485f8e2
Source noteuspto-grants-2013_09