HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46663Generated: October 29, 2026
Hydrogen Sulfide → HCID 20386626, compound
https://huagongshe.com/reaction/46663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 20386676 | HCID 20386676 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 20386626 | HCID 20386626 | — |
Reaction Steps
In a 1-liter autoclave were place 30 g (82.8 mmoles) of 1,2-diphenyl-4-(3-fluoro-4-methoxyphenyl)butane-1,4-dione, 100 ml of xylene, 18.4 g (41.4 mmoles) of phosphorus pentasulfide and 130 g of hydrogen sulfide. The vessel was heated 205 minutes at 155°-163` C. (1145-1235 psig.). The reactor was cooled and the hydrogen sulfide vented into a solution of 200 g of sodium hydroxide in 2 l of water. The semisolid residue was stirred with 150 ml of absolute ethanol. Filtration gave a first crop of 14.7 g (49.3%) m.p. 122°-125° C. Chilling the filtrate and refiltration gave a second crop of 10.5 g (35.2%), m.p. 118°-122° C. The two crops were combined and recrystallized from a mixture of 30 ml of dioxane and 70 ml of absolute ethanol to give 21.5 g (72.0%) of colorless plates, m.p. 123°-125° 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-4a509ab6fc884d158987810cf62608f7 |
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| Source note | uspto-grants-1979_11 |
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