HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46656Generated: October 29, 2026
Hydrogen Sulfide → 2,3-Di-p-anisyl-5-p-chlorophenylthiophene
https://huagongshe.com/reaction/46656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 57264742 | HCID 57264742 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2,3-Di-p-anisyl-5-p-chlorophenylthiophene | HCID 86736701 | 153.3% |
Reaction Steps
In a 1-liter stainless steel autoclave equipped with stirrer were placed 54.5 g (0.133 mole) of 1,2-di-p-anisyl-4-p-chlorophenylbutane-1,4-dione, 100 ml of xylene and 30 g (0.0675 mole) of phosphorus pentasulfide. The autoclave was cooled with a Dry Ice-acetone bath and 130 g (3.81 moles) of hydrogen sulfide was distilled into the autoclave. The vessel was stirred and heated for three hours at 162°-168° C. (1220-1290 psig). After cooling to room temperature the hydrogen sulfide was vented into an aqueous sodium hydroxide solution. Treatment with 150 ml of absolute ethanol to remove unreacted phosphorus pentasulfide gave 77 g of crude product. Recrystallization from 400 ml of absolute ethanol gave 45 g (83.1%) of pure 2,3-di-p-anisyl-5-p-chlorophenylthiophene, m.p. 125°-128° 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-57d05772f0d3420799e83c85b730f450 |
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| Source note | uspto-grants-1979_11 |
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