HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446892Generated: October 26, 2026
Chloromethyl Methyl Ether → 4,5-dichloro-2-methoxymethyl-2H-pyridazin-3-one
https://huagongshe.com/reaction/446892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | 4,5-Dichloro-3-hydroxypyridazine | HCID 73247 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,5-dichloro-2-methoxymethyl-2H-pyridazin-3-one | HCID 12351834 | 583.7% |
Reaction Steps
4,5-Dichloro-2H-pyridazin-3-one (30 g, 182 mmol), N,N-diisopropylethylamine (47.5 mL, 258 mmol) and 4-dimethylaminopyridine (2.20 g, 18.2 mmol) were dissolved in 200 mL of methylene chloride, to which was slowly added dropwise chloromethyl methyl ether (16.6 mL, 21.8 mmol) while maintaining at 0° C. The mixture was stirred for 3 h at room temperature. The reaction solution was washed with saturated aqueous sodium hydrogen carbonate solution, distilled under reduced pressure, and separated-purified by column chromatography (10% methylene chloride/ethyl acetate) to give the title compound (26.6 g, Yield: 70%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481537B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-1e8a5b17c8074463a49096be65b85ec9 |
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| Source note | uspto-grants-2013_07 |
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