HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373588Generated: October 30, 2026
1-(3-Chlorophenyl)piperazine → HCID 19810680, compound
https://huagongshe.com/reaction/373588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(3-Chlorophenyl)piperazine | HCID 1355 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-N-trityl-1-propanamine | HCID 256581 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19810680 | HCID 19810680 | 105.5% |
Reaction Steps
A mixture of 5.9 g (30 mmol) of 1-(3-chlorophenyl)piperazine, 12.55 g (33 mmol) of 3-bromo-N-(triphenylmethyl)propanamine, 6.2 g (45 mmol) of potassium carbonate and 60 ml of dimethylformamide is stirred at 90° C. for 6.5 h under argon. The mixture is then poured into iced water and is extracted with ethyl acetate. The organic phase is separated off, is washed with water, is dried and the solvent is evaporated off. 15.7 g of oily residue are obtained and are purified by chromatography on a column of silica gel by eluting with a 99/1 dichloromethane/methanol mixture, which yields 11.8 g of light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05164397 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-e3c920a3bcb142418c69e20935593b80 |
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| Source note | uspto-grants-1992_11 |
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