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HRID 1821667생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1821667

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Methoxy-5-methylphenolHCID 14519—
반응물3,6-Dichloropyridazine 1-oxideHCID 260910—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
용매1,4-DioxaneHCID 31275—
생성물6-Chloro-3-(2-methoxy-5-methylphenoxy)pyridazine 1-oxideHCID 2294001670.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07608563B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-1b8cca4cc3cd466abd35091009dc7e40
출처 메모uspto-grants-2009_10