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HRID 3339作成日:2026年10月24日

Sodium hydride → (1-Benzyl-2-methyl-1H-indol-4-yloxy)-acetic acid methyl ester

https://huagongshe.com/ja/reaction/3339

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Methyl bromoacetateHCID 60984—
反応物1-Benzyl-2-methyl-1H-indol-4-olHCID 10752360—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物(1-Benzyl-2-methyl-1H-indol-4-yloxy)-acetic acid methyl esterHCID 1080481988%

反応手順

4-Hydroxy-2-methyl-1-(phenylmethyl)-1H-indole (530 mg, 2.2 mmol) was added to 88 mg (2.2 mmol) of 60% NaH/mineral oil in 20 mL of DMF and the mixture stirred for 0.67 hours. Then, 0.21 mL (2.2 mmol) of methyl bromoacetate was added and stirring maintained for 17 hours. The mixture was diluted with water and extracted with ethyl acetate. The ethyl acetate solution was washed with brine, dried (MgSO4), and concentrated at reduced pressure. The residue was chromatographed on silica gel eluting with 20% EtOAc/hexane to give 597 mg (88% yield) of [[2-methyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]acetic acid methyl ester, 140°-143° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733923
出典データセットuspto-grants-1998_03
ORD IDord-19b0abee38be4025b9f496f094d7d0bd
出典メモuspto-grants-1998_03