HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635789Generated: November 1, 2026
Potassium Hydroxide → Benzene, 1,1'-thiobis[3-(phenylthio)-
https://huagongshe.com/reaction/635789
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 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 |
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| Patent number | US06191080B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-e1a62cd2ac3a4e5296af8c10cd3448c4 |
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| Source note | uspto-grants-2001_02 |
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