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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856072Generated: October 27, 2026

p-Bromochlorobenzene → Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/856072

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
ReactantEthyl AcetateHCID 8857—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylateHCID 149150386%

Reaction Steps

A mixture of p-bromochlorobenzene (1.91 g, 9.99 mmol), tert-butyl 4-aminopiperidine-1-carboxylate (2.0 g, 9.99 mmol), palladium acetate (45 mg, 0.2 mmol), (R)-(+)-BINAP (187 mg, 0.3 mmol) and sodium tert-butoxide (1.35 g, 14.0 mmol) in toluene (20 ml) was refluxed under a nitrogen atmosphere for 1 hour. Ethyl acetate and water were added to the reaction mixture while stirring, the insoluble substances were removed by filtration through Celite, and the filtrate was then extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/methanol=100/1) to afford tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate (2.67 g, yield 86%) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-c276d8dff44d4683981ae2411bdadb15
Source noteuspto-grants-2007_08