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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710597Generated: October 27, 2026

tert-Butyl 4-(2-methoxy-5-nitrophenyl)piperazine-1-carboxylate → Tert-butyl 4-(5-amino-2-methoxyphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1710597

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(2-methoxy-5-nitrophenyl)piperazine-1-carboxylateHCID 18180062—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(5-amino-2-methoxyphenyl)piperazine-1-carboxylateHCID 10686178—

Reaction Steps

33 g of 4-(2-Methoxy-5-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (97.8 mmol) were dissolved in 450 mL of methanol. 3 g of 10% Pd/C were added at room temperature under nitrogen atmosphere, and the reaction mixture was hydrogenated for 4 h. The reaction mixture was filtered over Celite, the was solvent evaporated and the remaining residue was treated with 100 mL of diisopropylether. Once crystallization started, the solvent was removed under reduced pressure and the remaining product dried thoroughly. This material was used in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790727B2
Source datasetuspto-grants-2010_09
ORD IDord-bcdd356ba6e74c68a46abd02d7f4913c
Source noteuspto-grants-2010_09