HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268116Generated: November 2, 2026
Thionyl Chloride → 3-(4-Methoxybenzyloxy)-N-(2-sulfamoylphenyl)benzamide
https://huagongshe.com/reaction/1268116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Aminobenzenesulfonamide | HCID 72894 | — |
| Reactant | 3-(4-Methoxybenzyloxy)benzoic acid | HCID 17607351 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-(4-Methoxybenzyloxy)-N-(2-sulfamoylphenyl)benzamide | HCID 12041319 | 31% |
Reaction Steps
A benzene (30 ml) solution containing 4.00 g (15.5 mmol) of 3-(4-methoxybenzyloxy)benzoic acid and 3 ml of thionyl chloride was heated under reflux for 2 hours and then the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in methylene chloride (30 ml), this solution was added dropwise under ice-cooling to a pyridine (50 ml) solution containing 2.93 g (17.0 mmol) of 2-aminobenzenesulfonamide, the mixture was stirred at room temperature for 18 hours and then methylene chloride was evaporated under a reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with a 1 N hydrochloric acid aqueous solution, water and saturated brine in that order and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The thus obtained residue was purified by a silica gel chromatography to obtain 1.5 g (yield: 31.0%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06555584B1 |
|---|
| Source dataset | uspto-grants-2003_04 |
|---|
| ORD ID | ord-a8bd65a0433342d6b3a939c176ea6134 |
|---|
| Source note | uspto-grants-2003_04 |
|---|