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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432597Generated: October 30, 2026

Water → Tert-butyl 4-(4-cyano-3-fluorophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/432597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-DifluorobenzonitrileHCID 77545—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 4-(4-cyano-3-fluorophenyl)piperazine-1-carboxylateHCID 5455253630%

Reaction Conditions

Temperature150 °C

Reaction Steps

2,4-Difluorobenzonitrile (5.00 g, 35.94 mmol), tert-butyl-1-piperazinecarboxylate (6.69 g, 35.92 mmol) and potassium carbonate (10.0 g, 72.4 mmol) were combined in dimethylsulfoxide (40 mL) and stirred at 150° C. overnight. The reaction mixture was cooled to ambient temperature, poured into water (150 mL) and extracted into ethyl acetate (150 mL). The extract was washed twice with water and once with brine, dried over magnesium sulfate and concentrated. The residue was purified by flash chromatography (2″×5″ silica gel). The column was flushed with 500 mL each 10% and 20% ethyl acetate/hexane and the product removed with an additional 500 mL of 20% ethyl acetate/hexane. Concentration gave 4-(4-cyano-3-fluoro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester as a white solid (3.28 g, 30%) which had mp 130.5-131.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664258B1
Source datasetuspto-grants-2003_12
ORD IDord-7024e669a7c3485aa0f7428d7cc7ce1a
Source noteuspto-grants-2003_12