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HRID 9666作成日:2026年10月24日

3-Methylthiophene → Thiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-

https://huagongshe.com/ja/reaction/9666

反応式

関与物質

役割名称HCID仕込み量
反応物3-MethylthiopheneHCID 12024—
反応物Benzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒TetrahydrofuranHCID 8028—
生成物Thiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-HCID 21986373—

反応条件

温度0 °C

反応手順

To a solution of 3-methylthiophene (2.31 ml) in anhydrous THF (75 ml) at −78° C. under N2 was added dropwise n-BuLi (1.6 M in hexanes, 15 ml). Thirty minutes after the addition was complete, the reaction mixture was allowed to warm to 0° C. and stirred for a further 30 minutes. Zinc chloride (0.5 M in THF, 48 ml) was added drop-wise, after a further 15 minutes palladium (0) tetrakis(triphenylphosphine) (100 mg) and 4-bromobenzotrifluoride (3.36 ml) were added and the reaction allowed to attain room temperature. The reaction mixture was warmed to 40° C. and stirred at this temperature for 3 hours. The reaction mixture was then cooled to room temperature and the solvents removed in vacuo. The residue was partitioned between and ether and the aqueous extract further washed with ether. The combined organic extracts were dried (MgSO4), filtered and evaporated to yield a brown oil. Purification by Biotage® chromatography eluting with cyclohexane yielded the title compound as a white 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-15ae2bc802194632a49a178c7691a128
出典メモuspto-grants-2006_08