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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267928Generated: October 31, 2026

Dimethyl Sulfoxide → Tert-butyl 4-(3-methyl-4-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1267928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-nitrotolueneHCID 94956—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(3-methyl-4-nitrophenyl)piperazine-1-carboxylateHCID 5376399797.7%

Reaction Steps

4-Fluoro-2-methyl-1-nitrobenzene (2 g), piperazine-1-carboxylic acid tert-butyl ester (4.8 g), potassium carbonate (3.57 g) and dimethyl sulfoxide (20 ml) were heated together at 80° C. under nitrogen for 15 hours. The mixture was then cooled, diluted with ethyl acetate (200 ml), washed with 2M aqueous hydrochloric acid (200 ml), dried (MgSO4), and concentrated to give the sub-title compound (4.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555541B1
Source datasetuspto-grants-2003_04
ORD IDord-3e4f8af0f8224988a756ecc1dcb62e2a
Source noteuspto-grants-2003_04