HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968873Generated: October 30, 2026
p-Chlorothiophenol → (4-Chlorophenyl)(2,5-difluorobenzyl)sulfane
https://huagongshe.com/reaction/968873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(Bromomethyl)-1,4-difluorobenzene | HCID 522830 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-Chlorophenyl)(2,5-difluorobenzyl)sulfane | HCID 16681304 | 99.6% |
Reaction Steps
4-Chlorothiophenol (253 g, 1.75 mol) was dissolved in industrial methylated spirits (1265 mL) and 2M sodium hydroxide solution (901 mL) was added, maintaining the temperature below 20° C. A solution of 2,5-difluorobenzyl bromide (355 g, 1.72 mol) in industrial methylated spirits (250 mL) was added dropwise to the thiolate solution, maintaining the temperature below 15° C. Upon completion of the reaction, water (1000 mL) was added. The resulting slurry was aged at 5° C. and then filtered. The cake was washed sequentially with cold industrial methylated spirits:water (40:60) and then water (500 mL). Drying in vacuo at ambient temperature furnished 2-[[(4-chlorophenyl)thio]methyl]-1,4-difluorobenzene (462.3 g, 99.6%). 1H NMR (CDCl3)—as obtained for the corresponding intermediate of Method (a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07304094B2 |
|---|
| Source dataset | uspto-grants-2007_12 |
|---|
| ORD ID | ord-3289849961524ec8aa07781e642056d9 |
|---|
| Source note | uspto-grants-2007_12 |
|---|