Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cinnamylpiperazine | HCID 86803 | — |
| Reactant | HCID 57133902 | HCID 57133902 | — |
| Product | HCID 70573063 | HCID 70573063 | — |
Reaction Steps
A mixture of 10.45 g (0.052 mole) of 1-cinnamylpiperazine, 29.2 g (0.104 mole) of bis(p-fluorophenyl)methyl-2-chloroethyl ether, 12.5 g (0.09 mole) of potassium carbonate, 2 g (0.012 mole) of potassium iodide and 250 ml of methyl isobutyl ketone was refluxed for 24 hours. The precipitate was filtered off and the filtrate was concentrated by evaporation of the solvent. Water and diethyl ether were added to the residue, the ethereal phase was separated off and dried over sodium sulphate. Then an ethereal maleic acid solution was added until the reaction mixture was acidic. The resulting precipitate was filtered off and recrystallized from a mixture of isopropyl alcohol and diethyl ether. 1-{2-[Bis(p-fluorophenyl)methoxy]ethyl}-4-(3-phenylprop-2-enyl)piperazine maleate (1:2) was obtained. It melted at 192°-194° C. The hydrochloride (1:2) melts at 211.5°-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04265894 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-8179e688d3c64a7ba004ff3114c6ac23 |
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| Source note | uspto-grants-1981_05 |
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