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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38250Generated: October 30, 2026

Tert-butyl 4-(2-chloro-4-nitrophenyl)piperazine-1-carboxylate → Tert-Butyl 4-(4-Amino-2-Chlorophenyl)Piperazine-1-Carboxylate

https://huagongshe.com/reaction/38250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(2-chloro-4-nitrophenyl)piperazine-1-carboxylateHCID 18783805—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
ProductTert-Butyl 4-(4-Amino-2-Chlorophenyl)Piperazine-1-CarboxylateHCID 1878376698.4%

Reaction Steps

According to Scheme 5 Step 2: A solution of tert-butyl 4-(2-chloro-4-nitrophenyl)piperazine-1-carboxylate (2.50 mmol, 854 mg) in EtOH (450 mL) was passed through a Pt/C 5% column in an H-Cube equipment (mode: Full). Then the solution was concentrated under reduced pressure to yield tert-butyl 4-(4-amino-2-chlorophenyl)piperazine-1-carboxylate (2.46 mmol, 766 mg, 98%). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524726B2
Source datasetuspto-grants-2013_09
ORD IDord-0430052d69e14b47b0487cbcc89409c9
Source noteuspto-grants-2013_09