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HRID 343533作成日:2026年10月26日

Ethyl bromoacetate → 3-Cyano-3-(3,4-dimethylphenyl)pentanedioic acid diethyl ester

https://huagongshe.com/reaction/343533

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物2-(3,4-Dimethylphenyl)acetonitrileHCID 76401—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Cyano-3-(3,4-dimethylphenyl)pentanedioic acid diethyl esterHCID 53845428—

反応条件

温度5 °C

反応手順

Combine 3,4-dimethylphenylacetonitrile (50.0 mmol) and tetrahydrofuran (140 mL). Cool to about 5° C. Add dropwise a solution of sodium bis(trimethylsilyl)amide (800 mL, 1M in tetrahydrofuran, 800 mmol). When the addition is complete, warm the reaction mixture to ambient temperature and allow to stir for 1 hour. Transfer the above solution via cannula into a cooled (-8° C.) solution of ethyl bromoacetate (84.5 mL, 762 mmol) in tetrahydrofuran (500 mL) at such a rate that the temperature of the reaction mixture does not rise above 20° C. Allow to stir at ambient temperature. After 18 hours, dilute with diethyl ether (1.5 L) and extract with saturated aqueous solution of ammonium chloride, then water, and then saturated aqueous solution of sodium chloride. Dry the organic layer over MgSO4, filter, and concentrate invacuo to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05861417
出典データセットuspto-grants-1999_01
ORD IDord-130399e8c95d4e54a6ab3f2ada24a2e8
出典メモuspto-grants-1999_01