HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(2,4-dimethoxybenzyl)-3,4-difluorobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Reactant | 3,4-Difluorobenzene-1-sulfonyl chloride | HCID 2736913 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,4-dimethoxybenzyl)-3,4-difluorobenzenesulfonamide | HCID 89962551 | 100% |
Reaction Steps
To a solution of 2,4-dimethoxybenzylamine (3.35 mL, 22.3 mmol) and pyridine (9.02 mL, 111.5 mmol) in dichloromethane (75 mL), 3,4-difluorobenzenesulfonyl chloride (3.04 mL, 22.3 mmol) was added with cooling on ice, and the reaction solution was stirred at room temperature for 16 hours. To the reaction solution, 2 M hydrochloric acid (100 mL) was added, and an organic layer was extracted. The thus obtained organic layer was dried over anhydrous sodium sulfate and vacuum concentrated to yield the title compound (7.66 g, 99%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889741B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-96b055b881cc4de09baae01a2ea3a2b1 |
| Source note | uspto-grants-2014_11 |