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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273996생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/273996

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참여 물질

역할이름HCID투입량
반응물3-(Bromomethyl)benzoic acidHCID 245650—
반응물3,4-Dimethoxy-alpha[(4-methylphenyl)thio]benzeneacetonitrileHCID 10542167—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물3-[2-Cyano-2-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]ethyl]benzoic acidHCID 1059889785.1%

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387685
출처 데이터셋uspto-grants-1995_02
ORD IDord-260917c3a7ef4014bb2b71352417c94a
출처 메모uspto-grants-1995_02