HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583541Generated: October 31, 2026
1-Bromo-3-chloropropane → HCID 13424606, compound
https://huagongshe.com/reaction/1583541
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3,4-Dimethoxyphenyl)piperazine | HCID 2736207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13424606 | HCID 13424606 | — |
Reaction Steps
The 1-(3-chloropropyl-4-(3,4-dimethoxyphenyl)piperazine is prepared in the following manner: 11.5 g (70.2 m. moles) of 1-bromo-3-chloropropane are added quickly with stirring to a mixture of 13 g (58.5 m. moles) of 1-(3,4-dimethoxyphenyl)piperazine [prepared according to P. C. Jain et coll. J. Med. Chem. 10, 812 (1967)] and 9.7 g (70.2 m. moles) of potassium carbonate in 60 cc of N,N-dimethylformamide. The stirring is continued for 4 hours 30 min at ambient temperature. The inorganic products are then filtered and the filtrate concentrated to dryness under reduced pressure. The residue is dissolved in ether and the solution obtained washed with water, then dried on sodium sulfate. After evaporation of the ether, there is obtained 14 g (yield) 80%) of 1-(3-chloropropyl)-4-(3,4-dimethoxyphenyl)piperazine that is used without any other purification.
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-8031d95b2d2544168610f4226ae53ffe |
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| Source note | uspto-grants-1985_11 |
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