Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031663Generated: October 29, 2026

Acetyl chloride → N-(4-Acetyl-5-methoxy-2-phenoxyphenyl)methanesulfonamide

https://huagongshe.com/reaction/1031663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantN-(5-Methoxy-2-Phenoxyphenyl)methanesulfonamideHCID 10803650—
SolventDichloromethaneHCID 6344—
ProductN-(4-Acetyl-5-methoxy-2-phenoxyphenyl)methanesulfonamideHCID 1472229386%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954518
Source datasetuspto-grants-1990_09
ORD IDord-02b5f74f4b244e99b34c69f82750439e
Source noteuspto-grants-1990_09