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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3-(Phenylsulfanyl)benzene-1-thiolHCID 53711390—
ReactantHCID 70018155HCID 70018155—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductBenzene, 1,1'-thiobis[3-(phenylthio)-HCID 75450—

Reaction Conditions

Temperature210 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191080B1
Source datasetuspto-grants-2001_02
ORD IDord-e1a62cd2ac3a4e5296af8c10cd3448c4
Source noteuspto-grants-2001_02