Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | HCID 13852600 | HCID 13852600 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13648719 | HCID 13648719 | 30.4% |
Reaction Steps
To 200 ml of water were added 31.0 g of 2-tert.-butyl-4,5-dibromo-3(2H)-pyridazinone and 15.8 g of 70% sodium hydrosulfide. After stirring at 60° C. for 4 hours, the resulting mixture was allowed to cool to room temperature and incorporated with about 8 ml of concentrated hydrochloric acid to lower the pH of the liquid to not higher than 2. The resulting solid was filtered off, washed with water, dried and then recrystallized from benzene/n-hexane to give 8.0 g of the intended product as white crystals of m.p. 107°-110° C. (yield: 30.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04877787 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-48e0a2d377c7479c9e644d004df6c49c |
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| Source note | uspto-grants-1989_10 |
|---|