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HRID 1386437作成日:2026年10月27日

Ethyl 2-(4-methoxyphenoxy)-6-[3,4-(methylenedioxy)phenoxy]benzoate → 2-[(2H-1,3-Benzodioxol-5-yl)oxy]-6-(4-methoxyphenoxy)benzoic acid

https://huagongshe.com/reaction/1386437

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-(4-methoxyphenoxy)-6-[3,4-(methylenedioxy)phenoxy]benzoateHCID 15540784—
反応物Sodium hydroxide ethanolHCID 23692425—
生成物2-[(2H-1,3-Benzodioxol-5-yl)oxy]-6-(4-methoxyphenoxy)benzoic acidHCID 1587234180.9%

反応手順

NaOH/EtOH (0.5 M) was added to ethyl 2-(4-methoxyphenoxy)-6-[3,4-(methylenedioxy)phenoxy]benzoate (175 mg, 0.429 mmol) at 25° C. The mixture (solid and solution) was heated under reflux for 20 hr. until TLC indicated the absence of starting material and the formation of a polar material. The solvent was evaporated and the residue was diluted with H2O (7 ml, pH≈7.5) and extracted with EtOAc (2×7 ml) to give 132 mg 2-(4-methoxyphenoxy)-6-[3,4-(methylenedioxy)phenoxy]benzoic acid as a yellow foam which was recrystallized from MeOH/H2O (twice) to give 102 mg of colorless needles, m.p. 164-165° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06265428B1
出典データセットuspto-grants-2001_07
ORD IDord-00ca68f9507f4b65b99dd1a3971ec781
出典メモuspto-grants-2001_07