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HRID 548549作成日:2026年10月25日

{4-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid methyl ester → {4-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid

https://huagongshe.com/reaction/548549

反応式

関与物質

役割名称HCID仕込み量
反応物{4-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid methyl esterHCID 67157962—
溶媒EthanolHCID 702—
溶媒Sodium HydroxideHCID 14798—
生成物{4-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acidHCID 57581228—

反応手順

A solution of {4-[3-(3,5-dibromo-phenyl)-prop-2-ynyloxy]-2-methyl-phenoxy}-acetic acid methyl ester (207 mg, 0.44 mmol) in ethanol (50 ml) and 1N NaOH (5 ml) was stirred at 75° C. for 30 min. The reaction mixture was evaporated and the residue dissolved in water (10 ml). Aqueous 1N HCl (5 ml) was added and the mixture was extracted with methylene chloride (3×10 ml). The combined organic phases were dried and evaporated to give the title compound in 187 mg (93%) yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943612B2
出典データセットuspto-grants-2011_05
ORD IDord-6515416561a44982ad42fdb62364dddf
出典メモuspto-grants-2011_05