HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704524Generated: October 27, 2026
Potassium Carbonate → 1-(4-Chlorobenzoyl)-1-(4-methylpiperazin-1-yl)-cyclopropane
https://huagongshe.com/reaction/704524
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-Bromo-4-chloro-1-(4-chlorophenyl)butan-1-one | HCID 107167 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Chlorobenzoyl)-1-(4-methylpiperazin-1-yl)-cyclopropane | HCID 13711684 | 50.3% |
Reaction Steps
A solution of 29.6 g (0.1 mol) of 4-chlorophenyl 1-bromo-3-chloropropyl ketone in 30 ml of dimethylformamide is added dropwise to a mixture of 10.4 g of N-methyl piperazine and 14 g of potassium carbonate in 30 ml of dimethylformamide at room temperature. Stirring is continued for 3 hours, after which a solution of 9 g of potassium hydroxide in 30 ml of methanol is added dropwise. The reaction mixture is stirred for a further hour at 50 C. and evaporated down in vacuo. The residue is taken up in ethyl acetate/water, and the organic phase is separated off, washed with water, dried over sodium sulphate and evaporated down in vacuo. The residue is chromatographed over silica gel using chloroform/ethanol (97:3). 14 g (50.3% of theory) of 1-(4-chlorobenzoyl)-1-(4-methylpiperazin-1-yl)-cyclopropane are obtained as a reddish oil, which can be directly used further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988382 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-c130781f8c794b21a72adedb7ba6921f |
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| Source note | uspto-grants-1991_01 |
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