HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392787Generated: November 3, 2026
Toluene → 2'-Sulfamoyl-biphenyl-4-carboxylic acid
https://huagongshe.com/reaction/1392787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Carboxyphenylboronic Acid | HCID 312183 | — |
| Reactant | 2-Bromobenzenesulfonamide | HCID 2801263 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2'-Sulfamoyl-biphenyl-4-carboxylic acid | HCID 2760555 | 57.4% |
Reaction Steps
2-Bromobenzenesulfonamide (800 mg) and 4-carboxyphenylboronic acid (563 mg) were suspended in a mixed solvent of toluene (5 ml) and water (5 ml). Tetrakis(triphenylphosphine)palladium (392 mg) and anhydrous sodium carbonate (1.08 g) were successively added to the suspension, and the mixture was heated under reflux overnight. After the reaction mixture was cooled to room temperature, diethyl ether and water were added to conduct liquid separation. The resultant organic layer was extracted twice with water. The resultant water layers were all combined, and 12N hydrochloric acid was added to this solution to acidify it. The solution was concentrated to about 20 ml under reduced pressure. Colorless powder deposited was collected by filtration and dried under reduced pressure to obtain the title compound (539 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342014B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-bc99965c81c849a19ec6aa2d5ce765e5 |
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| Source note | uspto-grants-2008_03 |
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