HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46662Generated: October 29, 2026
Hydrogen Sulfide → 2,3-Diphenyl-5-p-methoxyphenylthiophene
https://huagongshe.com/reaction/46662
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-p-methoxyphenylbutane-1,4-dione | HCID 2733039 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3-Diphenyl-5-p-methoxyphenylthiophene | HCID 54091294 | 142.8% |
Reaction Steps
In a 1-liter steel autoclave fitted with a mechanical stirrer, a thermometer and a pressure gauge were placed 32 g (0.09 mole) of 1,2-diphenyl-4-p-methoxyphenylbutane-1,4-dione, 100 ml of xylene, 20 g (0.045 mole) of phosphorus pentasulfide and 130 g of hydrogen sulfide. The mixture was stirred and heated 3 hours at 157°-162° C. (1190-1220 psig). The vessel was cooled and the hydrogen sulfide vented into an aqueous sodium hydroxide trap. The semisolid residue was stirred with 150 ml of absolute ethanol. Filtration gave 23 g (72%) of crude product, m.p. 130°-132° C. and a second crop of 3.7 g (11.6%) m.p. 124°-126° C. The two crops were combined and recrystallized from a mixture of 30 ml of dioxane and 60 ml of absolute ethanol to give 22 g (69%) of pure product m.p. 133°-134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04174405 |
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| Source dataset | uspto-grants-1979_11 |
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| ORD ID | ord-3d4393c5c73f41ff80a02d1f48faa88f |
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| Source note | uspto-grants-1979_11 |
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