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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415086Generated: October 26, 2026

Tert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylate → Tert-butyl 4-(3,4-diaminophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/415086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylateHCID 22272542—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(3,4-diaminophenyl)piperazine-1-carboxylateHCID 1878378985.8%

Reaction Steps

A 500 ml Parr hydrogenation flask was charged with tert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylate (9.0 g), methanol (250 mL) and 10% palladium on carbon (50% w/w water, 2.0 g). The atmosphere of the vessel was replaced by hydrogen gas. The reaction was shaken under a hydrogen atmosphere at 40 psi at room temperature for 1 hour. The reaction mixture was filtered through a plug of Celite, which was washed with additional methanol. The filtrate was concentrated at reduced pressure and the residue was triturated with ether to give 7.0 g of tert-butyl 4-(3,4-diaminophenyl)piperazine-1-carboxylate (yield 85%). 1H-NMR (400 MHz, MeOH-d4): δ 6.65 (d, 1H), 6.47 (s, 1H), 6.30 (d, 1H), 3.52 (s, 4H) 2.90 (s, 4H), 1.48 (s, 9H). MS (EI) for: 293 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088767B2
Source datasetuspto-grants-2012_01
ORD IDord-075baf869d2b4204a1fd4e5f3ea4481d
Source noteuspto-grants-2012_01