HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354443Generated: November 1, 2026
Hydrochloric Acid → 3-[5-(4-Trifluoromethylphenyl)-3-isoxazolyl]benzoic acid
https://huagongshe.com/reaction/1354443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 3-[5-(4-trifluoromethylphenyl)-3-isoxazolyl]benzoate | HCID 22934533 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[5-(4-Trifluoromethylphenyl)-3-isoxazolyl]benzoic acid | HCID 21105737 | 88% |
Reaction Steps
A mixture of methyl 3-[5-(4-trifluoromethylphenyl)-3-isoxazolyl]benzoate (1.04 g), 1 M aqueous sodium hydroxide solution (10 ml), tetrahydrofuran (30 ml) and methanol (30 ml) was stirred at 60° C. for 1 hr. After cooling, the reaction mixture was poured into water, and 1 M hydrochloric acid (20 ml) was added. The crystals were collected by filtration and recrystallized from ethanol to give 3-[5-(4-trifluoromethylphenyl)-3-isoxazolyl]benzoic acid (0.876 g, yield 88%) as a colorless crystalline powder. melting point: 276–277° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07223791B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-e04cf371646b41d3b5a349076f2b42f4 |
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| Source note | uspto-grants-2007_05 |
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