HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737145Generated: October 25, 2026
4-Bromobenzyl bromide → 1-(4-Bromo-benzyl)-3-isopropyl-piperazine
https://huagongshe.com/reaction/737145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | 2-(Propan-2-yl)piperazine | HCID 558976 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(4-Bromo-benzyl)-3-isopropyl-piperazine | HCID 57849456 | — |
Reaction Steps
0.7 g of 2-isopropyl-piperazine could be dissolved in acetonitrile and cooled to 0° C. A solution of 0.5 quiv. 4-bromobenzylbromide in acetonitrile could be added dropwise over 1 h. The reaction would be stirred at room temperature for 2 h. The reaction mixture could be concentrated and the residue could be purified by column chromatography (silica, eluent dichloromethane, 0-5% methanol, 0-0.5% dimethylethylamine) to afford 1-(4-bromo-benzyl)-3-isopropyl-piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07595397B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-ab84154b14f74b55ad5a7dce6f1af402 |
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| Source note | uspto-grants-2009_09 |
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