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HRID 549605作成日:2026年10月26日

(4-Ethynylphenyl)methanol → {4-[3-[2-(4-Chloro-phenyl)-ethoxy]-5-(4-hydroxymethyl-phenylethynyl)-phenylsulfanyl]-2-methylphenoxy}-acetic acid ethyl ester

https://huagongshe.com/reaction/549605

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Ethynylphenyl)methanolHCID 11170993—
反応物(4-{3-Bromo-5-[2-(4-chloro-phenyl)-ethoxy]-phenylsulfanyl}-2-methyl-phenoxy)acetic acid ethyl esterHCID 57791905—
触媒Copper iodideHCID 83717—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
生成物{4-[3-[2-(4-Chloro-phenyl)-ethoxy]-5-(4-hydroxymethyl-phenylethynyl)-phenylsulfanyl]-2-methylphenoxy}-acetic acid ethyl esterHCID 67024299—

反応手順

(4-{3-Bromo-5-[2-(4-chloro-phenyl)-ethoxy]-phenylsulfanyl}-2-methyl-phenoxy)acetic acid ethyl ester (270 mg; 0.46 mmol), (4-ethynyl-phenyl)-methanol (296 mg; 2.2 mmol), bis(triphenylphosphine) palladium (II) chloride (31.4 mg; 0.045 mmol) and copper iodide (6.4 mg; 0.034 mmol) were dissolved in a mixture of triethylamine (2 mL) and DMF (2 mL) under an atmosphere of nitrogen. The reaction mixture was reacted in a microwave oven at 110° C. for 1.5 h. The reaction mixture was evaporated to dryness, and 5% aqueous citric acid (30 mL) and ethyl acetate (30 mL) was added. The two phases were separated and the aqueous phase was extracted with ethyl acetate (30 mL). The combined organic phases were dried and evaporated to dryness and purified by preparative HPLC (method B). Yield: 270 mg (83%). HPLC-MS: m/z: 587.1 (M+H)+; Rt: 2.96 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943669B2
出典データセットuspto-grants-2011_05
ORD IDord-40fe545e37db488dbc623052b9b86667
出典メモuspto-grants-2011_05