HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42335Generated: October 29, 2026
Tert-Butylamine → N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide
https://huagongshe.com/reaction/42335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 2-Fluoro-4-methylbenzenesulphonyl chloride | HCID 2778482 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide | HCID 11107608 | — |
Reaction Steps
To an ice cooled solution of tert-butylamine (12.55 ml) in THF (60 ml) was added a solution of 2-fluoro-4-methylbenzene-1-sulfonyl chloride (5 g) in THF (25 ml), dropwise. After stirring for 15 min at 0° C., the reaction mixture was allowed to warm and stirred at room temperature for 2 hours. The HCl salt was removed by filtration and the filtrate was concentrated to give a yellow residue, which was triturated with Et2O and Hexanes to give 5.10 g N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide as an off-white granular solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536187B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-a7424409105145a4ae3d3ec5c4cf105f |
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| Source note | uspto-grants-2013_09 |
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