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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743693Generated: October 26, 2026

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

https://huagongshe.com/reaction/743693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(4-Nitrophenyl)piperazineHCID 3380696—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 1101130170.3%

Reaction Steps

A suspension of 4-(N-tert-butyloxycarbonyl-N'-piperazinyl)-1-nitrobenzene (3.09 g) in ethanol (70 ml) was hydrogenated at 30 psi for 15 min, in the presence of a palladium on carbon catalyst (0.35 g, 11% (w/w)). The catalyst was filtered off and the residue evaporated in vacuo. The resultant oil was azeotroped with toluene (2×20 ml) followed by petrol (60/80) (20 ml) to afford the aniline (1.96 g). 1H NMR (360 MHz, CDCl3) δ 1.48 (9H, s), 2.96-2.98 (4H, m), 3.56-3.59 (4H, m), 6.65 (2H, d, J=8.7), 6.81 (2H, d, J=8.7 Hz). MS (CI, NH3) 278 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556969
Source datasetuspto-grants-1996_09
ORD IDord-1cfbe140cd4e42719b57e1cc61b43cf5
Source noteuspto-grants-1996_09