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HRID 1445890作成日:2026年10月27日

Sodium hydride → 2-[1-(12-Bromo-dodecyl)-2-methyl-1H-indol-4-yloxy]-3-methylbutyric acid ethyl ester

https://huagongshe.com/reaction/1445890

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1,1-DibromododecaneHCID 11324906—
反応物3-Methyl-2-(2-methyl-1H-indol-4-yloxy)-butyric acid ethyl esterHCID 59170396—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-[1-(12-Bromo-dodecyl)-2-methyl-1H-indol-4-yloxy]-3-methylbutyric acid ethyl esterHCID 68547745—

反応手順

To a mixture of NaH (60% in mineral oil, 0.42 g, 10 mmole) in anhydrous DMF (20 mL), 3-methyl-2-(2-methyl-1H-indol-4-yloxy)-butyric acid ethyl ester (2) (1.88 g, 7.0 mmole) and dibromododecane (2.30 g, 7.0 mmole) were added. The mixture was stirred at room temperature for 18 h. The reaction was diluted with ethyl acetate (50 mL) and washed with water (3×30 mL). The organic layer was separated, dried over sodium sulphate and concentrated. The residue was purified by column chromatography (10:1 Hex:EtOAc) to afford intermediate (3) Yield: intermediate (3) 1.32 g, 35%, by-product (4) 1.56 g, 31%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07666898B2
出典データセットuspto-grants-2010_02
ORD IDord-b67f5df1629e4f6887454f4c59b9e5e0
出典メモuspto-grants-2010_02