HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395240Generated: October 25, 2026
Ethanol → 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine maleate
https://huagongshe.com/reaction/1395240
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]piperazine | HCID 9974013 | — |
| Product | 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine maleate | HCID 25009462 | — |
Reaction Steps
To a mixture of 6 g (0.018 mol) of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]piperazine (prepared as described in Example 3) and 3 g of potassium carbonate powder in 50 ml of ethanol, 3.6 g (0.018 mol) of (3-bromopropyl) benzene (G.O. Aspinall et al., J.Chem.Soc.1950, 743) was added dropwise at room temperature. The mixture was then slowly heated and refluxed for 3 hours. The reaction mixture was filtered and the filtrate was concentrated. The residue was taken up in diethyl ether, undissolved matter was filtered off and ethereal maleic acid was added until the liquid reacted acidic. The precipitate was filtered off and crystallized from a mixture of methanol and dimethylformamide. 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine maleate (1:2) was obtained. Melting point 185.0°-185.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202896 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-10f2db6e61094661942ede8a07b2279d |
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| Source note | uspto-grants-1980_05 |
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