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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361792Generated: October 31, 2026

Potassium Phosphate, Tribasic → (2-(4-Chloro-phenyl)-2-[4-(1H-pyrazol-4-yl)-phenyl]-ethyl)-methyl-amine

https://huagongshe.com/reaction/2361792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
Reactant[2-(4-Bromo-phenyl)-2-(4-chloro-phenyl)ethyl]-methyl-amineHCID 57691393—
CatalystHCID 178418851HCID 178418851—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(2-(4-Chloro-phenyl)-2-[4-(1H-pyrazol-4-yl)-phenyl]-ethyl)-methyl-amineHCID 1143835384.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of [2-(4-Bromo-phenyl)-2-(4-chloro-phenyl)-ethyl]-methyl-amine (6.1 g, 13.716 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (5.3 g, 27.431 mmol) and K3PO4 (10.19 g, 48.00 mmol) in ethanol (7.5 ml), methanol (11.5 ml), toluene (7.5 ml) and water (11.5 ml) was purged with nitrogen for 2 minutes. Bis(tri-t-butylphosphine)palladium (0) (175 mg, 2.5 mol %) was then added and the reaction mixture purged with nitrogen for a further 2 minutes. The mixture was then heated to 80° C., under nitrogen for a period of 17 hours. The solvents were removed and the residue was partitioned between ethyl acetate and 2N NaOH. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with brine, dried (MgSO4) and concentrated under reduced pressure. The crude reaction mixture was purified by column chromatography (SiO2), eluting with dichloromethane:methanol:acetic acid:water (90:18:3:2) to afford the title compound (3.6 g); LCMS (PS-A2) Rt 2.08 min [M+H]+ 312.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691806B2
Source datasetuspto-grants-2014_04
ORD IDord-bbd615d60c054b31a3362fa20b52dab3
Source noteuspto-grants-2014_04