HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46666Generated: November 3, 2026
Hydrogen Sulfide → HCID 20386623, compound
https://huagongshe.com/reaction/46666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 20386683 | HCID 20386683 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 20386623 | HCID 20386623 | 61.9% |
Reaction Steps
In a 1-l stainless steel autoclave were placed 56.2 g (0.150 mole) of 1,2-diphenyl-4-(2,4-dimethoxyphenyl)butane-1,4-dione, 100 ml of xylene, 33.3 g (0.075 mole) of phosphorus pentasulfide and 120 g of hydrogen sulfide. The contents of the autoclave were stirred at 160°-162° C. (1040-1080 psig) for three hours. The autoclave was then cooled, and the remaining hydrogen sulfide was vented into a trap of aqueous sodium hydroxide. The residue was stirred with 150 ml of absolute ethanol to destroy excess phosphorus pentasulfide. Chilling to -78° C. and filtration gave 27.6 g (49.4%) of crude product, m.p. 107°-110° C. Recrystallization from 30 ml of dioxane and 60 mll of ethanol gave 17.3 g (31%) of pure 2,3-diphenyl-5-(2,4-dimethoxyphenyl)thiophene, m.p. 112°-114° 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-dab0657f93fa4b42ba3a1fe5153c2d75 |
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| Source note | uspto-grants-1979_11 |
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