HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzenesulfonyl chloride → 4-fluorobenzenesulfinic acid sodium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | 4-Fluorothiophenol | HCID 67789 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Product | 4-fluorobenzenesulfinic acid sodium salt | HCID 23666220 | — |
Reaction Steps
It has now been found that 4-fluorothiophenol can be prepared in an advantageous manner if 4-fluorobenzenesulphonyl chloride is first reacted with sodium hydrogen sulphite solution to give a solution of sodium 4-fluorobenzenesulphinate, then this solution is reduced with sulphur dioxide to give 4,4'-difluorodiphenyl disulphide and this is finally reacted with sodium borohydride in a water-miscible inert organic solvent to give 4-fluorothiophenol (sodium salt). 4-Fluorothiophenol can be isolated from this sodium salt solution after distilling off the solvent, for example by acidifying the solution, separating off the organic phase forming and if appropriate purifying still further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05659088 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-0d89c01f87304cff9af996fc48a5ec42 |
| Source note | uspto-grants-1997_08 |