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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503837Generated: October 31, 2026

Cesium carbonate → Tert-butyl 4-(3-fluoro-4-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1503837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBinap, (A+-)-HCID 634876—
Reactant4-Bromo-2-fluoro-1-nitrobenzeneHCID 2783362—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(3-fluoro-4-nitrophenyl)piperazine-1-carboxylateHCID 66738172—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-bromo-2-fluoro-1-nitrobenzene (5 g, 23 mmol), tert-butyl piperazine-1-carboxylate (4.24 g, 23 mmol), palladium diacetate (0.51 g, 2.3 mmol), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (2.13 g, 3.4 mmol) and cesium carbonate (14.8 g, 45 mmol) in toluene (120 mL) was heated under nitrogen at 60° C. for 20 hours. After cooling to ambient temperature, the mixture was concentrated and the residue was diluted with dichloromethane (300 mL) and washed with water. The combined organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography on silica gel (200-300 mesh) eluting with 3/1 petroleum ether/ethyl acetate to give the title compound. MS: 348 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212192B2
Source datasetuspto-grants-2015_12
ORD IDord-00247088b5204658aeb726e825d46038
Source noteuspto-grants-2015_12