HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 2,3-Diphenyl-5-o-chlorophenylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 53746567 | HCID 53746567 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2,3-Diphenyl-5-o-chlorophenylthiophene | HCID 53925826 | 67.3% |
Reaction Steps
A 1-liter stainless steel stirred autoclave was charged with 33 g. (0.0946 mole) of 1,2-diphenyl-4-o-chlorophenylbutane-1,4-dione, 100 ml. of xylene, 20 g of phosphorus pentasulfide and 125 g of hydrogen sulfide. The autoclave was then heated at 160°-187° C. for three hours. The autoclave was cooled and vented. The residue was washed with ethanol and filtered off to give 17 g (51.8%) of crude product, m.p. 103°-107° C. Recrystallization from 20 ml of dioxane and 40 ml of ethanol gave 10.5 g (32%) of pure product, m.p. 117°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-7753e8950ee947498c91a91e32258812 |
| Source note | uspto-grants-1979_11 |