HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414006Generated: November 1, 2026
Water → 1-(3-Chlorophenyl)-4-(3-chloropropyl)-piperazine
https://huagongshe.com/reaction/1414006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(3-Chlorophenyl)piperazine monohydrochloride | HCID 25681 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(3-Chlorophenyl)-4-(3-chloropropyl)-piperazine | HCID 101444 | 9% |
Reaction Steps
To a solution fo 7.36 g. (0.184 mole) of sodium hydroxide in 75 ml. of water and 75 ml. of acetone there is added 17.16 g. (0.074 mole) of 1-(3-chlorophenyl)piperazine hydrochloride and 11.59 g. (0.074 mole) of 1-bromo-3-chloropropane, and the resulting mixture is stirred at 27° for 18 hrs. The organic layer is then separated and concentrated to an oil under reduced pressure. The oil is treated with hot (85°) 6 N HCl until solution is complete, and the resulting solution is filtered and stored at 5° for 18 hrs. The precipitate which forms is collected on a filter to afford 17.52 g. (87%) of the hydrochloride salt of the product, m.p. 198°-200°. Concentration of the mother liquor under reduced pressure and recrystallization of the residue from water affords an additional 1.82 g (9%) of product, m.p. 196°-198°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04252806 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-c7af2029361c420c8a72a17142596603 |
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| Source note | uspto-grants-1981_02 |
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