HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-fluoro-N-{4-fluoro-3-nitrophenyl}benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | 4-Fluoro-3-nitroaniline | HCID 67768 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-fluoro-N-{4-fluoro-3-nitrophenyl}benzenesulfonamide | HCID 798928 | 80.7% |
Reaction Steps
Pyridine (500 uL, 6.19 mmol) was added to a solution of 4-fluoro-3-nitro-phenylamine (1 g, 6.41 mmol) and 4-fluoro-benzenesulfonyl chloride (1.2 g, 6.19 mmol) in dichloromethane (DCM) (20 mL) and the reaction was stirred at room temperature overnight. The reaction was then partitioned between water and DCM. The organic layer was washed several times with water and concentrated. Recrystalization from ethanol/water gave 1.57 g of the sub-title compound as tan crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732618B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-6f17df37e00a4352aac9ba84d1fdc378 |
| Source note | uspto-grants-2010_06 |