HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849488Generated: October 26, 2026
Piperazine → 5-Chloro-2-(piperazin-1-yl)benzonitrile
https://huagongshe.com/reaction/849488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2,5-Dichlorobenzonitrile | HCID 89000 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Chloro-2-(piperazin-1-yl)benzonitrile | HCID 19367127 | 20.5% |
Reaction Steps
A mixture of 2,5-dichlorobenzonitrile (Lancaster; 2.994 g), piperazine (Aldrich; 7.616 g), and DMF (10 mL) is stirred for 4.5 h at 100° C. After cooling, the DMF is removed under reduced pressure and the residue is partitioned between dichloromethane and saturated aq. sodium bicarbonate. The organic layers are dried with MgSO4 and concentrated under reduced pressure. The residue is chromatographed on silica gel using methanol/dichloromethane (8/92) and the appropriate fractions are combined and concentrated to give 0.79 g of 5-chloro-2-(piperazin-1-yl)benzonitrile; MS m/z 221; IR (mineral oil) 1489, 802, 829, 2223, 845 cm-1, 1H NMR (CDCl3) δ 3.09, 3.18, 6.94, 7.43, 7.52.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06013654 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-22c467f1d577466d9788be631f81d645 |
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| Source note | uspto-grants-2000_01 |
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