Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32161Generated: October 25, 2026

Potassium Phosphate, Tribasic → (R)-1-butyl-4-[2-(4,4-dimethylcyclohexyl)-4-(3-methoxypiperidin-1-yl)phenyl]piperazine

https://huagongshe.com/reaction/32161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Reactant1-[4-Bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazineHCID 23141738—
Reactant(3R)-3-methoxypiperidine hydrochlorideHCID 69216666—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
Product(R)-1-butyl-4-[2-(4,4-dimethylcyclohexyl)-4-(3-methoxypiperidin-1-yl)phenyl]piperazineHCID 5976938559.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-[4-bromo-2-(4,4-dimethylcyclohexyl)phenyl]-4-butylpiperazine (37.4 mg, 0.0918 mmol) produced in Example (21c), (R)-3-methoxypiperidine hydrochloride (16.7 mg, 0.110 mmol) produced in Example (49a), tripotassium phosphate (170 mg, 0.801 mmol), palladium(II) acetate (8.2 mg, 0.0365 mmol), tri-t-butylphosphonium tetrafluoroborate (32 mg, 0.110 mmol) and xylene (1.5 mL) was stirred for 4 hours and 30 minutes at an external temperature of 100° C. under a nitrogen atmosphere. The mixture was air-cooled to room temperature and then purified by NH silica gel column chromatography (ethyl acetate/hexane) to give 24 mg of (R)-1-butyl-4-[2-(4,4-dimethylcyclohexyl)-4-(3-methoxypiperidin-1-yl)phenyl]piperazine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425554B2
Source datasetuspto-grants-2008_09
ORD IDord-1059d9599d9f45f89d302d12e19044cb
Source noteuspto-grants-2008_09