HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351548Generated: October 31, 2026
Water → Ethyl 4-[4-(4-hexyloxyphenyl)piperazin-1-yl]benzoate
https://huagongshe.com/reaction/351548
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzoic acid, 4-fluoro-, ethyl ester | HCID 67976 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 1-(4-Hexyloxyphenyl)piperazine dihydrochloride | HCID 22713162 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 4-[4-(4-hexyloxyphenyl)piperazin-1-yl]benzoate | HCID 22713156 | — |
Reaction Steps
To a suspension of 1-(4-hexyloxyphenyl)piperazine dihydrochloride (0.914 g) and potassium bicarbonate (0.564 g) in dimethylsulfoxide (5 ml) was added ethyl p-fluorobenzoate (0.2 ml) and stirred for 10 hours at 150° C. The reaction mixture was added to a mixture of water and ethyl acetate. The organic layer was taken and dried over magnesium sulfate. The magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure to give ethyl 4-[4-(4-hexyloxyphenyl)piperazin-1-yl]benzoate (0.347 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743776B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-20d7321285604218920836b49b28c70c |
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| Source note | uspto-grants-2004_06 |
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