HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006235Generated: November 1, 2026
Heptane → 1,3-Bis[4-[4-(3,4,5-trimethoxyphenyl)benzoyl]-1-piperazinyl]propane
https://huagongshe.com/reaction/1006235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Heptane | HCID 8900 | — |
| Reactant | 3,4,5-Trimethoxybenzeneboronic acid | HCID 2734390 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1,3-Bis[4-(4-bromobenzoyl)-1-piperazinyl]propane | HCID 11692723 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,3-Bis[4-[4-(3,4,5-trimethoxyphenyl)benzoyl]-1-piperazinyl]propane | HCID 10440293 | 92% |
Reaction Steps
In toluene (200 mL)-methanol (50 mL) were dissolved 50.0 g (86.5 mmol) of 1,3-bis[4-(4-bromobenzoyl)-1-piperazinyl] propane and 42.16 g (199 mmol) of 3,4,5-trimethoxyphenylboronic acid. The mixture was degassed with nitrogen. A solution of 9.35 g (173 mmol) of sodium methoxide in methanol (150 mL) was added in portions, then a solution of 9.35 g (173 mmol) of sodium methoxide in methanol (150 mL) and a solution of 970 mg (4.32 mmol) of palladium(II) acetate in toluene (150 mL) were added dropwise simultaneously over about 1 hour. After stirring for 1 hour at room temperature, 9.2 g of activated carbon was added and the mixture was stirred under hydrogen for 3 hours at room temperature. Insoluble materials were filtered off by filtration through Celite and the residue was washed with methanol-toluene (1:1,3×75 mL). The filtrate and the washings were combined and concentrated under reduced pressure, then water-isopropanol (5:1, 750 mL) was added. After stirring for 30 minutes at room temperature, precipitates were collected by filtration and washed with water-isopropanol (5:1, 3×100 mL) to obtain 65.6 g of crude crystals. To a suspension of the crude crystals (65.6 g) in methanol-tetrahydrofuran (1:2, 350 mL) stirred at 70° C. was added 3.3 g of activated carbon, and the mixture was stirred for 1.5 hours. Insoluble materials were filtered off at the same temperature and the residue was washed with hot methanol-tetrahydrofuran (1:2, 2×130 mL). The filtrate and the washings were combined and stirred at 70° C. to obtain a homogeneous solution, then heptane (390 mL) was added over about 1 hour. The mixture was stirred for 30 minutes at room temperature and for 1 hour in an ice bath. Precipitates were collected by filtration and washed with tetrahydrofuran-heptane (1:5, 3×130 mL) to obtain 59.48 g of 1,3-bis[4-[4-(3,4,5-trimethoxyphenyl)benzoyl]-1-piperazinyl] propane as a colorless crystalline powder (yield: 92%).mp: 192.0 to 193.5° C.
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-477e203b55b14d01a8b5eb85b93e28d5 |
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| Source note | uspto-grants-2004_09 |
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