HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626725Generated: November 3, 2026
Hydrochloric Acid → 5-Chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoic acid
https://huagongshe.com/reaction/1626725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 5-chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoate | HCID 66680385 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoic acid | HCID 46935554 | 41% |
Reaction Steps
0.61 g (1.7 mmol) of methyl 5-chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoate was dissolved in 20 mL of THF solvent, and 4 mL of 1N aqueous sodium hydroxide was added. The mixture was stirred at 50° C. for 1.5 hours. After cooling, 1N hydrochloric acid was added to acidify the reaction mixture. Thereafter, the solvent was distilled off under reduced pressure. Subsequently, water was added to the residue, and solids were collected by filtration and washed with water. The obtained crude product was recrystallized using a mixed solvent of ethyl acetate and n-hexane, thereby giving 0.24 g of the target 5-chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoic acid (yield: 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785473B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-38c31f20f81e485ab7bbb80efb220d58 |
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| Source note | uspto-grants-2014_07 |
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