Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12583976 | HCID 12583976 | — |
| Reactant | 2-tert-Butyl-5-hydroxy-4-methylpyridazin-3(2H)-one | HCID 54713106 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13825147 | HCID 13825147 | 69.7% |
Reaction Steps
To a solution of 0.9 g (0.005 mol) of 2-t-butyl-5-hydroxy-4-methyl-3(2H)-pyridazinone and 1.2 g (0.005 mol) of p-trimethylsilyl benzylbromide dissolved in 20 ml of N,N-dimethylformamide was added 1.0 g (0.007 mol) of potassium carbonate at room temperature under stirring. After addition, the resulting mixture was stirred at 120° C. for three hours. After allowed to cool, the reaction mixture was poured into 200 ml of water and extracted with 100 ml of benzene. The resulting benzene layer was washed with 100 ml of water, dried over anhydrous sodium sulfate, and freed of solvent by distillation to give 1.8 g of crude product. The crude product was recrystallized from 20 ml of hexane to obtain 1.2 g of 2-t-butyl-4-methyl-5-(p-trimethylsilyl benzyloxy)-3(2H)-pyridazinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04874861 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-256ff7dc361a4ff68863413698051125 |
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| Source note | uspto-grants-1989_10 |
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