HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → Benzene, 1,1'-thiobis[3-(phenylthio)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(Phenylsulfanyl)benzene-1-thiol | HCID 53711390 | — |
| Reactant | HCID 70018155 | HCID 70018155 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Benzene, 1,1'-thiobis[3-(phenylthio)- | HCID 75450 | — |
Reaction Conditions
| Temperature | 210 °C |
|---|
Reaction Steps
436 g of m-phenylmercapto thiophenol and 78 g of potassium hydroxide were dissolved in 500 ml of N-methyl-2-pyrrolidone, then 376 g of m-chlorophenyl phenylsulfide was added and the resultant mixture was heated to 170° C. After removing the water content, 20 g of cuprous chloride was added and heated to 210° C. and maintained at that temperature for 10 hours while stirring. After the reaction was over, the reaction product was treated by the same procedures as in Example Z-1 and bis(m-phenylmercaptophenyl)sulfide was obtained as a fraction at 255° C.-265° C./5 Torr by vacuum distillation. The product was referred as a comparative oil B and subjected to performance evaluation described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06586376B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-fec2aece0d034df2a9b756872eb9c27e |
| Source note | uspto-grants-2003_07 |