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HRID 590967作成日:2026年10月26日

Toluene → ethyl 2-hydroxy-2-(1-phenyl-1H-indol-2-yl)acetate

https://huagongshe.com/reaction/590967

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Ethyl oxoacetateHCID 70211—
反応物1-Phenyl-1H-indoleHCID 182029—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物ethyl 2-hydroxy-2-(1-phenyl-1H-indol-2-yl)acetateHCID 7081371219%

反応手順

A solution of butyllithium (1.6 M, 1.19 mL, 1.9 mmol) was added at −78° C. to a solution of 1-phenyl-1H-indole (5a) (350 mg, 1.81 mmol) in tetrahydrofuran (10 mL) under a nitrogen atmosphere. After 45 minutes, a solution of ethyl glyoxylate in toluene (50%, 400 μL, 2 mmol) was added. The reaction mixture was slowly warmed to room temperature for 12 hours, quenched with water (2 mL) and concentrated in vacuo. The residue was partitioned between dichloromethane (30 mL) and water (10 mL). The organic layer was washed with water (2×10 mL), brine (10 mL), dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 90/10) to afford the desired alcohol (5b) as a white solid (100 mg, 0.33 mmol, 19%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238026B2
出典データセットuspto-grants-2016_01
ORD IDord-e651d3765b184ad7b428914d243b832a
出典メモuspto-grants-2016_01