Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium bisulfide | HCID 102109 | — |
| Reactant | HCID 12246632 | HCID 12246632 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Potassium bisulfide | HCID 102109 | — |
| Product | HCID 178527974 | HCID 178527974 | — |
Reaction Steps
Potassium hydrosulfide methanolic solution is prepared by reacting 7 parts by weight of potassium hydroxide, 150 parts by volume of methanol and hydrogen sulfide gas in accordance with the known method. 4.2 parts by weight of 1,4-dichloro-7-phenyl-pyrido (3,4-d) pyridazine is added to the potassium hydrosulfide solution, and the resulting mixture is stirred at room temperature for three hours. Methanol is evaporated under reduced pressure, and the residue is added to 50 parts by volume of water to obtain a solution. The solution is acidified by the addition of acetic acid to precipitate yellow crystals. The crystals are collected by filtration, washed with water and dried to obtain 1,4-dimercapto-7-phenyl-pyrido (3,4-d) pyridazine melting at 212° to 215° C (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03998822 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-5045a22833cf4894922a130dbc4e2028 |
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| Source note | uspto-grants-1976_12 |
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