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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816740Generated: October 31, 2026

Cesium carbonate → 1-Acetyl-4-[4-(4-methoxy-4-phenylpiperidin-1-yl)phenyl]piperazine

https://huagongshe.com/reaction/1816740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantHCID 417384HCID 417384—
ReactantBinap, (A+-)-HCID 634876—
ReactantTrifluoromethanesulfonic acid 4-(4-acetylpiperazin-1-yl)phenyl esterHCID 22494772—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-4-[4-(4-methoxy-4-phenylpiperidin-1-yl)phenyl]piperazineHCID 2249471479.1%

Reaction Steps

A mixture of 1-acetyl-4-(4-trifluoromethanesulfonyloxyphenyl)piperazine (3 g), 4-methoxy-4-phenylpiperidine (1.63 g), acetic acid palladium(II) salt (0.11 g), racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.42 g) and cesium carbonate (3.88 g) in toluene (17 ml) was stirred for 30 minutes at ambient temperature. After being stirred for a further 17 hours at 100° C., the reaction mixture was diluted with dichloromethane. The suspension was filtered through celite, and the filtrate was evaporated under reduced pressure. The residue was purified by column chromatography over silica using ethyl acetate/methyl alcohol (30:1) as the elution to give 1-acetyl-4-[4-(4-methoxy-4-phenylpiperidin-1-yl)phenyl]piperazine (2.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884868B1
Source datasetuspto-grants-2005_04
ORD IDord-6cce7c9cc5d448bc90ed36f5d8764732
Source noteuspto-grants-2005_04