HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-(4-Acetyl-5-methoxy-2-phenoxyphenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-(5-Methoxy-2-Phenoxyphenyl)methanesulfonamide | HCID 10803650 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Acetyl-5-methoxy-2-phenoxyphenyl)methanesulfonamide | HCID 14722293 | 86% |
Reaction Steps
In 100 ml of anhydrous methylene chloride were dissolved 10 g of 3-methylsulfonylamino-4-phenoxyanisole and 2.81 g of acetyl chloride. Thereto was added 9.1 g of aluminum chloride in 5 minutes with ice-cooling. The mixture was stirred for 1 hour at 20°-25° C. The reaction mixture was introduced into 100 ml of ice water. The resulting organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried with anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was recrystallized from isopropyl alcohol to obtain 9.83 g (yield: 86%) of methyl 4-methylsulfonylamino-2-methoxy-5-phenoxyphenyl ketone having a melting point of 108.5-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04954518 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-02b5f74f4b244e99b34c69f82750439e |
| Source note | uspto-grants-1990_09 |