戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1821673作成日:2026年10月27日

2,6-Dimethylphenol → 6-Chloro-3-(2,6-dimethylphenoxy)pyridazine 1-oxide

https://huagongshe.com/reaction/1821673

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-DimethylphenolHCID 11335—
反応物1,4-DioxaneHCID 31275—
反応物3,6-Dichloropyridazine 1-oxideHCID 260910—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Dimethyl SulfoxideHCID 679—
生成物6-Chloro-3-(2,6-dimethylphenoxy)pyridazine 1-oxideHCID 2301380163.2%

反応手順

268 mg (2.20 mmol) of 2,6-dimethylphenol, 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL) were mixed, 270 mg (2.41 mmol) of potassium tert-butoxide was added to the mixture in an ice bath, and the resulting mixture was stirred for 10 minutes. To the mixture was added 370 mg (2.24 mmol) of 3,6-dichloropyridazine 1-oxide, and the resulting mixture was stirred at room temperature for 10 hours and allowed to stand for 2 days. The reaction mixture was poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed, and the residue was purified by silica gel column chromatography (hexane: ethyl acetate, gradient) to obtain 350 mg (1.39 mmol, Yield: 63.1%) of 6-chloro-3-(2,6-dimethylphenoxy)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-fb9040a4c4904a93b5f198518a099289
出典メモuspto-grants-2009_10