HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46655Generated: October 29, 2026
Hydrogen Sulfide → 2,3-Di-p-anisyl-5-p-tolylthiophene
https://huagongshe.com/reaction/46655
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 57279740 | HCID 57279740 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2,3-Di-p-anisyl-5-p-tolylthiophene | HCID 20386672 | — |
Reaction Steps
In a 1-liter stainless steel autoclave equipped with stirrer were placed 40.6 g (0.105 mole) of 1,2-di-p-anisyl-4-p-tolylbutene-1,4-dione, 100 ml of xylene and 25 g (0.056 mole) of phosphorus pentasulfide. The vessel was chilled with a Dry Ice-acetone bath and charged with 130 g (3.81 moles) of hydrogen sulfide. The autoclave was then heated with stirring for 215 minutes at 158°-165° C. (1250-1360 psig). After cooling the vessel, the hydrogen sulfide was allowed to vent into a sodium hydroxide solution. The residue was treated with 150 ml of absolute ethanol to destroy unreacted phosphorus pentasulfide. After removal of the ethanol there remained 70.5 g of crude product. Recrystallization from ethanol-dioxane (70:30) gave 20 g (49.3%) of pure 2,3-di-p-anisyl-5-p-tolythiophene, m.p. 99°-102° C. and a second crop of 6.5 g (16.0%) m.p. 92°-96° 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-cbf44bfcc2da40f6a16f47af255540fa |
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| Source note | uspto-grants-1979_11 |
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