HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737125Generated: October 31, 2026
4-Bromobenzoyl chloride → (4-Bromo-phenyl)-(3-phenyl-piperazin-1-yl)-methanone
https://huagongshe.com/reaction/737125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Reactant | 2-Phenylpiperazine | HCID 250673 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Bromo-phenyl)-(3-phenyl-piperazin-1-yl)-methanone | HCID 57849479 | — |
Reaction Steps
This compound could be made in the following manner: 500 mg of 2-phenylpiperazine would be dissolved in dichloromethane and cooled to 0° C. A solution of 0.5 equiv. of 4-bromobenzoyl chloride in dichloromethane would be added dropwise over 1 h at 0° C. The reaction would be stirred at 0° C. for 0.5 h, then allowed to warm to room temperature and stirred for a further 3 h until complete conversion. The reaction mixture would be diluted with dichloromethane, washed with 1M aqueous sodium hydroxide solution and brine, then dried over sodium sulfate, filtered and concentrated in vacuo. The crude residue would be purified by column chromatography to afford (4-bromo-phenyl)-(3-phenyl-piperazin-1-yl)-methanone.
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-9d7d4413c726459ea41f9b8dcbe5882c |
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| Source note | uspto-grants-2009_09 |
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