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HRID 1513106作成日:2026年10月26日

Benzene, 1-chloro-4-ethynyl- → {2-Chloro-4-[3-(4-chloro-phenylethynyl)-5-hydroxy-phenylsulfanyl]-phenoxy}-acetic Acid Ethyl Ester

https://huagongshe.com/reaction/1513106

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-chloro-4-ethynyl-HCID 70118—
反応物[4-(3-Bromo-5-hydroxy-phenylsulfanyl)-2-chloro-phenoxy]-acetic Acid Ethyl AcetateHCID 67024266—
触媒Copper iodideHCID 83717—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
生成物{2-Chloro-4-[3-(4-chloro-phenylethynyl)-5-hydroxy-phenylsulfanyl]-phenoxy}-acetic Acid Ethyl EsterHCID 57791919—

反応手順

[4-(3-Bromo-5-hydroxy-phenylsulfanyl)-2-chloro-phenoxy]-acetic acid ethyl acetate (1.1 g; 2.63 mmol), 4-chlorophenylacetylene (1.08 g; 7.9 mmol), bis(triphenylphosphine)-palladium (II) chloride (0.15 g; 0.21 mmol) and copper iodide (0.03 g; 0.16 mmol) were dissolved in a mixture of triethylamine (5 mL) and DMF (5 mL) under an atmosphere of nitrogen. The reaction mixture was reacted in a microwave oven at 100° C. for 1 h. The reaction mixture was evaporated to dryness and portioned between 5% aqueous citric acid and ethyl acetate. The organic phase was dried and evaporated to dryness. The crude product was purified by flash chromatography (ethyl acetate:heptane 1:3). Yield: 1.1 g. HPLC-MS: m/z: 473.3 (M+); Rt: 2.76 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08217086B2
出典データセットuspto-grants-2012_07
ORD IDord-3129ef06903c45f2b1c6ee01f62225e2
出典メモuspto-grants-2012_07