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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509088Generated: October 27, 2026

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

https://huagongshe.com/reaction/509088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant5-Fluoro-2-nitroanilineHCID 75399—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylateHCID 2227254282%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-fluoro-2-nitroaniline (10 g, 64.1 mmol) in DMF (65 mL) was added tert-butyl-piperazine carboxylate (13.1 g, 70.5 mmol) and K3PO4 (13.3 g, 96.2 mmol). The reaction mixture was stirred at 100° C. overnight. After adding 100 ml H2O into the solution, the precipitated yellow solid was filtered under vacuum then dried in vacuo to afford tert-butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylate as yellow solid (15 g, yield: 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096549B2
Source datasetuspto-grants-2015_08
ORD IDord-19c1eeebeab942babdd98ab1ccdfcac2
Source noteuspto-grants-2015_08