HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352023Generated: November 1, 2026
Water → 2-t-butyl-5-(p-fluorobenzyloxy)-4-methyl-3(2H)-pyridazinone
https://huagongshe.com/reaction/2352023
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzylic alcohol | HCID 68022 | — |
| Reactant | 2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-one | HCID 13822264 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-t-butyl-5-(p-fluorobenzyloxy)-4-methyl-3(2H)-pyridazinone | HCID 13825137 | 62.2% |
Reaction Steps
To a solution of 0.63 g (0.005 mol) of p-fluorobenzyl alcohol dissolved in 20 ml of N,N-dimethylformamide was added 0.24 g of 55% sodium hydride at room temperature under stirring. After addition, the resulting mixture was further stirred at room temperature for fifteen minutes. The reaction liquid was added dropwise with 1.0 g of 2-t-butyl-5-chloro-4-methyl-3(2H)-pyridazinone, and was stirred at room temperature for eight hours. The reaction mixture was poured into 200 ml of water and then extracted with 50 ml of benzene. The resulting benzene layer was washed successively with 50 ml of 10% sodium hydroxide, 50 ml of 1N-hydrochloric acid, and 100 ml of water, dried over anhydrous sodium sulfate, and freed of solvent by distillation to give 1.5 g of crude product. The crude product was recrystallized from 20 ml of hexane to obtain 0.9 g of 2-t-butyl-5-(p-fluorobenzyloxy)-4-methyl-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-b8c5a5d0778049ce95bddad55a7a06ec |
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| Source note | uspto-grants-1989_10 |
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