HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287638Generated: October 31, 2026
1-(3-Chlorophenyl)piperazine → HCID 18705621, compound
https://huagongshe.com/reaction/2287638
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(3-Chlorophenyl)piperazine | HCID 1355 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Naphthylalanine | HCID 185915 | — |
| Reactant | 1-(3-Chloropropyl)pyrrolidin-2-one | HCID 11105662 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 18705621 | HCID 18705621 | — |
Reaction Steps
A mixture of 1-chloro-3-[2-oxopyrrolidin-1-yl]propane (1 g, 6.2 mmcl), 1-(3-chlorophenyl)piperazine (1.22 g, 6.2 minol) anhydrous Na2CO3 (0.33 g, 3.1 mmol) and Nal (0.093 g, 0.6 mmcl) in dry xylene (15 ml) was stirred at 150° C. for 14 hours. The solvent was removed at reduced pressure and residue was poured on water (30 ml). The separated residue was extracted with dichloromethane (2×25 ml), dried over Na2SO4 and concentrated to give 1-[4-(3-chlorophenyl)piperazin-1-yl]-3-[3-oxopyrrolidin-1-yl]propane as an oil which was purified by flash column chromatography over silica gel using chloroform as fluent, yield 0.72 g (36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06084097 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-bb60aef93cef40d1abc8470ffd372faf |
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| Source note | uspto-grants-2000_07 |
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