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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973188Generated: October 31, 2026

Methanesulfonamide → N-methanesulfonyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetamide

https://huagongshe.com/reaction/973188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
ReactantSodiumHCID 5360545—
Reactant4-Chloro-α-[3-(trifluoromethyl)phenoxy]benzeneacetyl chlorideHCID 12109235—
SolventTetrahydrofuranHCID 8028—
ProductN-methanesulfonyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetamideHCID 54399462—

Reaction Conditions

Temperature20 °C

Reaction Steps

(3-Trifluoromethylphenoxy)(4-chlorophenyl)acetyl chloride (0.02 mole) in tetrahydrofuran (50 ml.) is added over a 15-minute period to a solution of the sodium salt of methanesulfonamide (2.5 g., 0.021 mole) in tetrahydrofuran (50 ml.) at 0°-5° C., under a nitrogen atmosphere. The mixture is stirred at 20° C. for 20 hours and then the solvent is evaporated under vacuum. The residue is dissolved in chloroform and the solution is extracted with water. The chloroform solution is dried over anhydrous magnesium sulfate, filtered and the solvent removed to afford N-methanesulfonyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055592
Source datasetuspto-grants-1977_10
ORD IDord-0bd7c8a44bae46cbb1d40663e8710c2c
Source noteuspto-grants-1977_10