HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Bromobenzenesulphonyl chloride → 3-Bromobenzene-1-sulfonyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Bromobenzenesulphonyl chloride | HCID 17943 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Bromobenzene-1-sulfonyl fluoride | HCID 70700039 | 81% |
Reaction Steps
To a stirred solution of 3-bromophenylsulfonyl chloride (5 g, 0.0196 mol) in acetonitrile (20 ml) was added potassium fluoride (2.27 g, 0.0391 mol) followed by 18-crown-6 ether (0.08 g) and the reaction stirred at room temperature for 18 h. The reaction mixture was then washed with water (60 ml), extracted with ethyl acetate (3×80 ml) and the combined organic extracts dried (Na2SO4). Solvents were evaporated in vacuo to give a yellow oil (3.79 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07439245B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-9e3770c8371746d9a4487f5b74a4a18e |
| Source note | uspto-grants-2008_10 |