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HRID 273996作成日:2026年10月26日

3-(Bromomethyl)benzoic acid → 3-[2-Cyano-2-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]ethyl]benzoic acid

https://huagongshe.com/reaction/273996

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Bromomethyl)benzoic acidHCID 245650—
反応物3,4-Dimethoxy-alpha[(4-methylphenyl)thio]benzeneacetonitrileHCID 10542167—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物3-[2-Cyano-2-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]ethyl]benzoic acidHCID 1059889785.1%

反応条件

温度-78 °C

反応手順

To a cold (-78° C.) solution of 1.86 g of 3,4-dimethoxy-α-[(4-methylphenyl)thio]benzene acetonitrile in 15 mL of tetrahydrofuran is added drop-wise a solution of 2.9 mL of n-butyl lithium (2.2 M) in hexane. This solution is stirred at -78° C. for 35 minutes. A solution of 0.67 g of m-carboxybenzyl bromide in 5 mL of anhydrous tetrahydrofuran is added drop-wise, stirred at -78° C. for 40 minutes and then at room temperature for 15 minutes. The mixture is quenched with water and extracted with ethyl acetate. The ethyl acetate extract is washed with brine, dried and filtered. The filtrate is evaporated in vacuo to yield a yellow oil. This oil is purified by flash chromatography using methylene chloride/methyl alcohol (95:5) to yield 1.15 g of the desired product as a yellow foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387685
出典データセットuspto-grants-1995_02
ORD IDord-260917c3a7ef4014bb2b71352417c94a
出典メモuspto-grants-1995_02