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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218866Generated: November 1, 2026

Water → Tert-butyl 4-(2-chloro-4-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2218866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventChloroformHCID 6212—
ProductTert-butyl 4-(2-chloro-4-nitrophenyl)piperazine-1-carboxylateHCID 1878380564.7%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3-chloro-4-fluoronitrobenzene (5 g, 27.1 mmol), 1-piperazinecarboxylic acid t-butyl ester (5 g, 26.8 mmol) and dimethylformamide (10 mL) was stirred for 3 hours and 30 minutes at an external temperature of 130° C. After adding water to the air-cooled reaction mixture, extraction was performed 3 times with chloroform. The organic layers were washed with brine and dried over anhydrous magnesium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/heptane) to give 5.93 g of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410971B2
Source datasetuspto-grants-2008_08
ORD IDord-72dde3c3504b4732801496770633b3d4
Source noteuspto-grants-2008_08