HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(3-Acetyl-4-chlorophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(5-amino-2-chlorophenyl)ethanone | HCID 1501911 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(3-Acetyl-4-chlorophenyl)methanesulfonamide | HCID 22141405 | — |
Reaction Steps
1-(5-Amino-2-chlorophenyl)ethanone (411 mg; synthesized by the process reported by Radziejewski et al., Heterocycles, vol. 26, pp. 1227-1238 (1987)) was dissolved in toluene (5 mL), and pyridine(235 μL) and methanesulfonyl chloride (225 μL) were added. The resulting mixture was stirred at room temperature for 50 minutes. After adding water (50 mL), the reaction mixture was extracted with ethyl acetate (500 mL). The organic layer was washed with an aqueous 1 N hydrochloric acid solution (50 mL) and saturated brine (50 mL) and then dried over anhydrous sodium sulfate (5 g). The solvent was distilled off under reduced pressure to yield the title compound (595 mg) as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06861444B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-e9196ed676cd4f29864faf165c320028 |
| Source note | uspto-grants-2005_03 |