HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 5-(3,4-Dichlorophenyl)-2,3-diphenylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | 1,2-Diphenyl-4-(3,4-dichlorophenyl)butane-1,4-dione | HCID 12488244 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(3,4-Dichlorophenyl)-2,3-diphenylthiophene | HCID 20386621 | 177.8% |
Reaction Steps
In a 1-liter stainless steel autoclave equipped with electrically-driven stirrer were placed 38.3 g. (0.100 mole) of 1,2-diphenyl-4-(3,4-dichlorophenyl)butane-1,4-dione, 100 ml of xylene, 20 g of phosphorus pentasulfide and 140 g of hydrogen sulfide. The reactor was heated for three hours at 160°-164° C. The crude product remaining after cooling and venting the reactor was stirred with ethanol. Filtration gave 30.5 g (80%) of solid m.p. 101°-103° C. Recrystallization from 30 ml of dioxane and 60 ml of ethanol gave 22.5 g (59%) of pure product, m.p. 106.2°-107.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-2f76414035bb4e89af3691c46890b0d9 |
| Source note | uspto-grants-1979_11 |