HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439251Generated: October 31, 2026
Phosphorus sulfide (P2S5) → 5-Pyrazin-2-yldithiole-3-thione
https://huagongshe.com/reaction/1439251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 21329209 | HCID 21329209 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Pyrazin-2-yldithiole-3-thione | HCID 182332 | 170.2% |
Reaction Steps
A mixture of 5-(pyrazin-2-yl)-1,2-dithiole-3-one (2 g.) and phosphorus pentasulphide (2.3 g.) in dioxan (35 cc.) is heated for 15 minutes at 100° C., whilst stirring. The red suspension obtained is diluted whilst hot with acetonitrile (35 cc.). The solution is decanted and the precipitate obtained is taken up with a hot mixture (2 × 50 cc.) of dioxan and acetonitrile (50:50 by volume). The combined organic phases are filtered hot, diluted with distilled water (250 cc.), and the requisite amount of a 4N aqueous ammonia solution to adjust the pH to 7. The brown precipitate formed is filtered off, washed with distilled water (2 × 25 cc.) and then with diethyl ether (2 × 10 cc.) and dried. 5-(Pyrazin-2-yl)-1,2-dithiole-3-thione (1.87 g.) melting at 200°-201° C. is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04058611 |
|---|
| Source dataset | uspto-grants-1977_11 |
|---|
| ORD ID | ord-2142235b40774844b130faded1e5f396 |
|---|
| Source note | uspto-grants-1977_11 |
|---|