HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583540Generated: October 31, 2026
1-Bromo-3-chloropropane → 1-(3-Fluorophenyl)piperazine
https://huagongshe.com/reaction/1583540
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Fluorophenyl)piperazine | HCID 77418 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3-Fluorophenyl)piperazine | HCID 77418 | — |
| Product | HCID 13312914 | HCID 13312914 | — |
Reaction Steps
The 1-(3-chloropropyl)-4-(3-fluorophenyl piperazine used is prepared in the following manner: 32 g (203 m. moles) of 1-bromo-3-chloropropane are added drop by drop to a mixture of 12.2 g (67.7 m. moles) Of 1-(3-fluorophenyl piperazine [prepared according to D. R. Maxwell and W. R. Wragg, English Pat. No. 943,739, C.A. 60, 5522c (1964)], 9.4 g (68 m. moles) of potassium carbonate and 135 cc of N,N-dimethylformamide. The stirring is continued for 9 hours at ambient temperature. The inorganic products are then removed by filtration, then the filtrate is concentrated under reduced pressure. The residue is dissolved in ether, the solution washed with a saturated solution of sodium chloride, then dried on sodium sulfate. The evaporation of the ether supplies an oil which is distilled (boiling1 =137°-140°). The 1-(3-chloropropyl)-4-(3-fluorophenyl)piperazine is obtained in the form of an oil that is crystallized in hexane. Yield: 11.6 g (67%), Melting point=48°-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04552878 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-1af4e7bb1b3e4c1ea1208ccd2d76947c |
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| Source note | uspto-grants-1985_11 |
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