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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014041Generated: October 30, 2026

Hydrochloric Acid → N-(2-Cyano-4-fluoro-phenyl)-methanesulfonamide

https://huagongshe.com/reaction/1014041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethanesulfonamideHCID 72879—
Reactant2,5-DifluorobenzonitrileHCID 123558—
SolventDimethyl SulfoxideHCID 679—
ProductN-(2-Cyano-4-fluoro-phenyl)-methanesulfonamideHCID 6687685934.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

(Step 1) A suspension of 2,5-difluorobenzonitrile (12.4 g), methanesulfonamide (9.3 g) and potassium carbonate (13.6 g) in DMSO (360 ml) was stirred overnight at 120° C. The reaction solution was poured into 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, and filtered. The solvent was evaporated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to give N-(2-cyano-4-fluorophenyl]methanesulfonamide (6.57 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982044B2
Source datasetuspto-grants-2011_07
ORD IDord-7abafcbf3cfb417eb1636fd53443e97e
Source noteuspto-grants-2011_07