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HRID 9692作成日:2026年10月24日

Acetic Acid → {2-Ethyl-4-[({2-methyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methyl)thio]phenoxy}acetic acid

https://huagongshe.com/ja/reaction/9692

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物DichlorodimethylsilaneHCID 6398—
反応物Ethyl 2-(4-(chlorosulfonyl)-2-ethylphenoxy)acetateHCID 21986343—
反応物[2-Methyl-5-(4-trifluoromethyl-phenyl)-furan-3-yl]-methanolHCID 21986436—
触媒ZincHCID 23994—
溶媒Ethyl AcetateHCID 8857—
生成物{2-Ethyl-4-[({2-methyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methyl)thio]phenoxy}acetic acidHCID 10225846—

反応条件

温度60 °C

反応手順

To a mixture of zinc (407 mg) in ethyl acetate (10 ml) stirred at 60° C. was added acetic acid (0.203 ml) followed by a solution of ethyl[4-(chlorosulfonyl)-2-ethylphenoxy]acetate (intermediate 111, 546 mg) in ethyl acetate. The reaction mixture was stirred 60° C. for 2 hours and then dichlorodimethylsilane (0.431 ml) was added drop-wise. After a further 90 minutes {2-methyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol (472 mg) was added and the reaction mixture stirred at reflux for 17 hours. The reaction mixture was diluted with ethyl acetate; extracted with water, saturated aqueous sodium bicarbonate, water and dried with brine and over sodium sulfate. An attempt was purify the crude material by Biotage® chromatography using 3:2 petroleum ether: ethyl acetate as eluent. The partially purified material (223 mg) was hydrolyzed in 1,4-dioxan (6 ml) using 0.5 M aqueous sodium hydroxide (1.86 ml) for 16 hours. The reaction mixture was neutralized with 50W×2-200 Dowex; evaporated and the residue purified by mass-directed autopreparative HPLC to give the title compound as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091237B2
出典データセットuspto-grants-2006_08
ORD IDord-226bde8a3698467aba4d78807100d28f
出典メモuspto-grants-2006_08