HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → HCID 54323588, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | 1,2-Diphenyl-4-p-bromophenylbutane-1,4-dione | HCID 20386747 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54323588 | HCID 54323588 | 117.1% |
Reaction Steps
A mixture of 31.4 g (0.080 mole) of 1,2-diphenyl-4-p-bromophenylbutane-1,4-dione, 100 ml of xylene, 16 g (0.036 mole) of phosphorus pentasulfide and 125 g (3.67 mole) of hydrogen sulfide was heated in a 1-liter stainless steel autoclave with stirring for four hours at 156°-176° C. (1140-1320 psig). The reactor was cooled to room temperature and the hydrogen sulfide was led into a sodium hydroxide solution. Treatment of the residue with 150 ml of absolute ethanol gave 18.5 g (59.1%) of crude solid, m.p. 135°-137°. Recrystallization from 20 ml of dioxane and 60 ml. of absolute ethanol gave 16.5 g (52.7%) of pure 2,3-diphenyl-5-p-bromophenylthiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-5cc2a4771eed4b1892d11bdcfaf31951 |
| Source note | uspto-grants-1979_11 |