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HRID 260651作成日:2026年10月27日

Diisopropylamine → 3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl ester

https://huagongshe.com/reaction/260651

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Ethyl 3-phenylpropionateHCID 16237—
反応物tert-Butyl bromoacetateHCID 79177—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl esterHCID 8674901246%

反応条件

温度-78 °C

反応手順

Dissolve diisopropylamine (3.5 mL, 25 mmol) in tetrahydrofuran (30 mL). Add n-butyllithium (14 mL of a 1.6M solution in hexane, 22.4 mmol). Stir for 15 minutes and cool to -78° C. Add, by dropwise addition, ethyl dihydrocinnamate (3.5 mL, 20 mmol) and stir for 30 minutes. Add t-butyl bromoacetate (4.0 mL, 25 mmol) and gradually warm to room temperature overnight. Quench the solution with ammonium chloride solution (10 mL) and partition between water (25 mL) and ethyl ether (50 mL). Separate the organic phase, dry (MgSO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography (5% ethyl acetate/hexane) to give 3-phenyl-2-t-butylcarboxymethylpropionic acid, ethyl ester as a pale yellow oil (2.68 g, 46%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05529997
出典データセットuspto-grants-1996_06
ORD IDord-c28dd0fd4efe467bb54bfbf4c7b8e4bf
出典メモuspto-grants-1996_06