HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268097Generated: October 31, 2026
Potassium Carbonate → HCID 12043041, compound
https://huagongshe.com/reaction/1268097
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Aminobenzenesulfonamide | HCID 72894 | — |
| Reactant | 3-(Benzyloxy)benzoic acid | HCID 309226 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 12043041 | HCID 12043041 | 90% |
Reaction Steps
A benzene (10 ml) solution containing 600 mg (2.3 mmol) of 3-benzyloxybenzoic acid and 1.5 ml of thionyl chloride was heated under reflux for 2 hours and then the solvent was evaporated. A dioxane (10 ml) solution of the resulting residue was added dropwise to a water-dioxane 1:1 (10 ml) solution containing 248 mg (1.44 mmol) of 2-amino-benzenesulfonamide and 726 mg (5.2 mmol) of potassium carbonate, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, dioxane was evaporated, the resulting residue was acidified by adding 1 N HCl under ice-cooling and extracted with ethyl acetate. The extract was washed with water and saturated brine and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. By recrystallizing the resulting residue from acetonitrile, 200 mg (yield: 90%) of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06555584B1 |
|---|
| Source dataset | uspto-grants-2003_04 |
|---|
| ORD ID | ord-08822bcd0ebb4415847052e8a166be1a |
|---|
| Source note | uspto-grants-2003_04 |
|---|