HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydrosulfide → 2-t-butyl-5-mercapto-4-methyl-3(2H)-pyridazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | 2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-one | HCID 13822264 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-t-butyl-5-mercapto-4-methyl-3(2H)-pyridazinone | HCID 13822265 | 96.7% |
Reaction Steps
To 75 ml of ethanol were added 17.0 g (0.085 mol) of 2-t-butyl-5-chloro-4-methyl-3(2H)-pyridazinone and 8.5 g (0.106 mol) of 70% sodium hydrosulfide and the mixture was stirred under reflax for 4 hours. After cooling, the mixture was poured into 300 ml of ice water and extracted with 200 ml of ethyl ether. The ether layer was washed with 100 ml of water, dried over anhydrous sodium sulfate and then freed of solvent by distillation to obtain 16.3 g of a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837217 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-a7b87b1a982d44db8a19ec7c8a410a02 |
| Source note | uspto-grants-1989_06 |