HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → N-(2-(o-Fluorobenzoyl)-4-nitrophenyl)-p-toluenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2-Amino-2'-fluoro-5-nitrobenzophenone | HCID 67657 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(2-(o-Fluorobenzoyl)-4-nitrophenyl)-p-toluenesulphonamide | HCID 3023542 | — |
Reaction Steps
A mixture containing 10 g of 2-amino-5-nitro-2'-fluorobenzophenone and 7.5 g of tosyl chloride is refluxed in 50 ml of pyridine for 24 hours. The solvent is evaporated off to dryness, water and ethyl acetate are added, an insoluble material is filtered off and the organic phase is washed with a dilute solution of hydrochloric acid, water and an aqueous solution of sodium chloride and then dried over magnesium sulfate and evaporated. The residue is chromatographed on silica and the expected product is eluted with DCM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05481005 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-3cd3151d66c7437c86a3b83b45c13a04 |
| Source note | uspto-grants-1996_01 |