HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl mercaptan → 2,4-Bis(benzylsulfanyl)-1,3,2lambda~5~,4lambda~5~-dithiadiphosphetane-2,4-dithione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | 1,4-Dichlorobenzene | HCID 4685 | — |
| Product | 2,4-Bis(benzylsulfanyl)-1,3,2lambda~5~,4lambda~5~-dithiadiphosphetane-2,4-dithione | HCID 22485820 | 50% |
Reaction Conditions
| Temperature | 190 °C |
|---|
Reaction Steps
The method is derived from the reference H. Davy, Sulfur Letters, vol. 3(2) 39, (1985). P4S10 (8.88 g, 0.02 mol) is mixed with 30 ml of dichlorobenzene until this solvent refluxes (160° C.). Benzylthiol (16.5 ml; 0.14 mol) is slowly added to the solution over 40 minutes, while increasing the temperature up to 190° C. The solution becomes clear; the reaction temperature is then reduced to 80° C. The stirring is stopped in order to allow the residual P4S10 to be separated by settling. The solution is filtered in the hot state. The product crystallizes slowly after filtration. The yield is 50%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890980B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-b47902b3e83446419b0d62d423f1baf4 |
| Source note | uspto-grants-2005_05 |