HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031654Generated: November 3, 2026
Water → N-(5-Methoxy-2-Phenoxyphenyl)methanesulfonamide
https://huagongshe.com/reaction/1031654
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5-METHOXY-2-PHENOXYANILINE | HCID 9429819 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(5-Methoxy-2-Phenoxyphenyl)methanesulfonamide | HCID 10803650 | 91.9% |
Reaction Steps
10.0 g of 3-amino-4-phenoxyanisole was dissolved in 50 ml of pyridine. Thereto was dropwise added 5.59 g of methanesulfonyl chloride in 10 minutes with ice-cooling. The mixture was stirred for 1 hour at 20°-25° C. The reaction mixture was introduced into a mixture of 200 ml of ethyl acetate and 100 ml of water. The resulting organic layer was separated and washed with three 100-ml portions of 2N hydrochloric acid and then with a saturated aqueous sodium chloride solution. The organic layer was separated, dried with anhydrous magnesium sulfate, and subjected to distillation under reduced pressure to remove the solvent. The resulting crystal was recrystallized from isopropyl alcohol to obtain 12.5 g (yield: 91.9%) of 3-methylsulfonylamino4-phenoxyanisole having a melting point of 109.5°-111° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04954518 |
|---|
| Source dataset | uspto-grants-1990_09 |
|---|
| ORD ID | ord-dc64d8a783fa4f1bab6cca134ccd6bd3 |
|---|
| Source note | uspto-grants-1990_09 |
|---|