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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006236Generated: October 31, 2026

Sodium Carbonate → 1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane

https://huagongshe.com/reaction/1006236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,3-Bis[4-(4-bromobenzoyl)-1-piperazinyl]propaneHCID 11692723—
Reactant4-Isopropoxy-3,5-dimethoxyphenylboronic acidHCID 22485594—
CatalystHCID 178418397HCID 178418397—
Product1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propaneHCID 1044079094%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under nitrogen were added 2.40 mL (48 mmol) of a 2 mol/L aqueous sodium carbonate solution and 729.9 mg (0.632 mmol) of tetrakis(triphenylphosphine)palladium (0) to a solution of 4.50 g (7.79 mmol) of 1,3-bis[4-(4-bromobenzoyl)-1-piperazinyl]propane and 4.50 g (18.7 mmol) of 4-isopropoxy-3,5-dimethoxyphenylboronic acid in ethanol-toluene (15 mL -60 mL), and the mixture was stirred for 3 hours at 80° C. The reaction mixture was concentrated under reduced pressure to remove the organic solvents. Water (15 mL) was added to the residue and the mixture was extracted with chloroform (100 mL, 3×30 mL). The organic layers were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel to give 5.93 g of 1,3-bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane as a colorless oil (yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787653B2
Source datasetuspto-grants-2004_09
ORD IDord-02ca2cf3049d4966a43346bf430d9afb
Source noteuspto-grants-2004_09