HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119342Generated: October 31, 2026
Potassium Carbonate → 1-(3,3-Diphenyl-propyl)-4-(4-nitro-benzyl)-[1,4]diazepane
https://huagongshe.com/reaction/2119342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | 1-(3,3-Diphenyipropyl)homopiperazine | HCID 23441035 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(3,3-Diphenyl-propyl)-4-(4-nitro-benzyl)-[1,4]diazepane | HCID 23441058 | — |
Reaction Steps
The resulting 1-(3,3-diphenylpropyl )homopiperazine was dissolved in 3 mL of acetonitrile followed by adding 213 mg of 4-nitrobenzyl bromide and 144 mg of potassium carbonate. The mixture was stirred at 70° C. for 14 hours and allowed to cool to room temperature and the solvent was removed under reduced pressure. 20 mL of aqueous 2N sodium hydroxide was added and the mixture was extracted with 20 mL×2 of ethyl acetate. The organic layers were combined, washed with 20 mL of saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, concentrated, and purified by column chromatography (silica gel, ethyl acetate) to obtain 255 mg of the titled compound. This was treated with a hydrogen chloride solution in ether and the solvent was removed under reduced pressure; and the residue was dried to obtain the hydrochloride salt of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06686353B1 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-b6d2b9ccf42d4f5fa0b1c36a3efc6012 |
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| Source note | uspto-grants-2004_02 |
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