HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → N-(4-Acetyl-2-methylphenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(4-Amino-3-methylphenyl)ethan-1-one | HCID 13355515 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-Acetyl-2-methylphenyl)methanesulfonamide | HCID 19873430 | — |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
4'-Amino-3'-methylacetophenone from Step VIII (3.0 g, 20 mmol) in 15 ml of dry pyridine at 5° C. is reacted with 3.0 g (26.2 mmol) of methanesulfonyl chloride in 5 ml of tetrahydrofuran. The reaction is stirred at 5° C. for 2 hrs, then at room temperature overnight. The reaction is diluted with ice-water. The solid is collected, washed with water, air dried and crystallized from methylene chloride-pet. ether to yield the title compound; m.p. 152°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155268 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-0ac4085aa85945ca8f78d814c4565448 |
| Source note | uspto-grants-1992_10 |