HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-Fluoro-N-(4-fluorophenyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Product | 4-Fluoro-N-(4-fluorophenyl)benzenesulfonamide | HCID 573540 | 78% |
Reaction Steps
To a solution of 4-fluorobenzenesulfonyl chloride (2 g, 10.3 mmol) at room temperature was stirred with pyridine (2.49 mL, 30.8 mmol) and 4-fluoroaniline (1.95 mL, 20.6 mmol) for 2 hrs. The reaction was quenched with 1 M HCl aqueous and then extracted with DCM, filtered through a phase separator and purified by silica gel column chromatography (0-100% DCM in cyclohexane) to give 4-fluoro-N-(4-fluoro-phenyl)-benzenesulfonamide (2.15 g, 78%). LCMS (m/z, Method A) ES+ 270 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09382222B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-674833a7699a48f6b10cb3365ed42dd9 |
| Source note | uspto-grants-2016_07 |