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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,3-Bis[4-(4-bromobenzoyl)-1-piperazinyl]propane | HCID 11692723 | — |
| Reactant | 4-Isopropoxy-3,5-dimethoxyphenylboronic acid | HCID 22485594 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane | HCID 10440790 | 94% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787653B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-02ca2cf3049d4966a43346bf430d9afb |
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| Source note | uspto-grants-2004_09 |
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