HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836807Generated: October 26, 2026
Tetrahydrofuran → 3-[4-(3,3-Diphenyl-1-propyl)piperazin-1-yl]benzoic acid
https://huagongshe.com/reaction/1836807
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 3-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]benzoate | HCID 22180549 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-[4-(3,3-Diphenyl-1-propyl)piperazin-1-yl]benzoic acid | HCID 22180487 | 85.6% |
Reaction Steps
The compound (2.00 g) prepared in step (b) was dissolved in a mixed solvent composed of tetrahydrofuran (20 ml) and methanol (10 ml), and a 1 mol/l aqueous sodium hydroxide solution (10 ml) was added to the solution. The mixture was then stirred at 65° C. for one hr. The solvent was removed from the reaction solution by distillation under the reduced pressure. Water (30 ml) was then added to the residue, and the mixture was adjusted to pH 4 by the addition of 1 mol/l hydrochloric acid. The resultant precipitate was collected by filtration, and was then dried to give 1.60 g (85.6%) of 3-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777414B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-5366cf7781da4955af2d0dd1fa1a4e6f |
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| Source note | uspto-grants-2004_08 |
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