HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-((4-fluoro-phenyl)-hydroxy-methyl)-benzenesulfonamide → 2-Chloro-5-(4-fluoro-benzoyl)-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-((4-fluoro-phenyl)-hydroxy-methyl)-benzenesulfonamide | HCID 58107495 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-5-(4-fluoro-benzoyl)-benzenesulfonamide | HCID 58107443 | 74.3% |
Reaction Steps
A solution of 65 mg of 2-chloro-5-((4-fluoro-phenyl)-hydroxy-methyl)-benzenesulfonamide in 1 mL of acetone is stirred at room temperature as 0.2 mL of 3 M Jones' reagent is added. The reaction mixture is stirred at room temperature for 30 minutes then diluted with ethyl acetate, filtered through celite, the filtrate is concentrated in vacuo. The crude product is purified by silica gel chromatography to give 48 mg of the title compound as white foam. 1H NMR (CDCl3): 5.15 (br, 2H), 7.12-7.30 (m, 3H), 7.70 (d, J=8 Hz, 1H), 7.80-7.90 (m, 2H), 7.90-8.0 (dd, 1H), 8.5 (d, J=2 Hz, 1H). MS (m/z): 312 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362063B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-021c5eb3bbb542eaa13848f86e5774e7 |
| Source note | uspto-grants-2013_01 |