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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-METHOXY-2-PHENOXYANILINEHCID 9429819—
SolventPyridineHCID 1049—
ProductN-(5-Methoxy-2-Phenoxyphenyl)methanesulfonamideHCID 1080365091.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954518
Source datasetuspto-grants-1990_09
ORD IDord-dc64d8a783fa4f1bab6cca134ccd6bd3
Source noteuspto-grants-1990_09