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HRID 1821667作成日:2026年10月27日

Water → 6-Chloro-3-(2-methoxy-5-methylphenoxy)pyridazine 1-oxide

https://huagongshe.com/reaction/1821667

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Methoxy-5-methylphenolHCID 14519—
反応物3,6-Dichloropyridazine 1-oxideHCID 260910—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Dimethyl SulfoxideHCID 679—
溶媒1,4-DioxaneHCID 31275—
生成物6-Chloro-3-(2-methoxy-5-methylphenoxy)pyridazine 1-oxideHCID 2294001670.2%

反応手順

In a mixed solvent of 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL) was dissolved 167.5 mg (1.21 mmol) of commercially available 2-methoxy-5-methylphenol, and 142.8 mg (1.27 mmol) of potassium tert-butoxide was added to the solution, then 202.9 mg (1.23 mmol) of 3,6-dichloropyridazine 1-oxide was added to the mixture and the resulting mixture was stirred at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was successively washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the obtained residue was purified by preparative thin-layer chromatography (available from MERCK CO., 1.05744, 3 plates were used, developed by ethyl acetate:hexane=2:1) to obtain 226.5 mg (0.849 mmol, Yield: 70.2%) of 6-chloro-3-(2-methoxy-5-methylphenoxy)pyridazine 1-oxide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07608563B2
出典データセットuspto-grants-2009_10
ORD IDord-1b8cca4cc3cd466abd35091009dc7e40
出典メモuspto-grants-2009_10