HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzenesulfonyl chloride → Benzenesulfonyl fluoride, 3-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzenesulfonyl chloride | HCID 8476 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Benzenesulfonyl fluoride, 3-nitro- | HCID 67683 | 86.4% |
Reaction Steps
3-Nitrobenzenesulphonyl chloride (10 g) was dissolved in 1,4-dioxane (30 ml) and stirred at room temperature. To this solution was added a solution of potassium fluoride (3.9 g) in water (5 ml) and the stirring continued at room temperature for 5 hours. The reaction mixture was allowed to stand at room temperature overnight and was poured into ice/water. The product was extracted into dichloromethane, the solvent was dried (MgSO4) and evaporated under reduced pressure to give the title compound (8 g). This material was sufficiently pure for the next stage of the synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856273 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-b6aef9a995ae42ac81fe40f748cce905 |
| Source note | uspto-grants-1999_01 |