HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015783Generated: October 27, 2026
Hydrochloric Acid → N-(2-Cyano-4-fluoro-phenyl)-methanesulfonamide
https://huagongshe.com/reaction/1015783
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 2,5-Difluorobenzonitrile | HCID 123558 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(2-Cyano-4-fluoro-phenyl)-methanesulfonamide | HCID 66876859 | 34.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985862B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-52a8dd9ef8c340ab8b8c4bf134ec1aeb |
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| Source note | uspto-grants-2011_07 |
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