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HRID 269953作成日:2026年10月27日

Dimethyl Sulfoxide → 2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl ester

https://huagongshe.com/reaction/269953

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物Potassium HydroxideHCID 14797—
反応物2-(1H-indol-4-yloxy)-2-methylpropionic acid ethyl esterHCID 16090870—
溶媒WaterHCID 962—
生成物2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl esterHCID 1609087398%

反応手順

2-(1H-Indol-4-yloxy)-2-methylpropionic acid ethyl ester (0.100 g, 0.40 mmol, 1.0 eq), powdered potassium hydroxide (0.034 g, 0.61 mmol, 1.5 eq), and DMSO (3 mL) were mixed and stirred at room temperature for 10 minutes. 1-Bromo-3-chloropropane (0.12 mL, 0.191 g, 1.21 mmol, 3.0 eq) was then added to the above mixture. The reaction mixture was stirred at room temperature for another 1.5 hours before 15 mL of water was added. The mixture was extracted with ethyl acetate (2×30 mL). The organic layer was collected, combined, washed with water (6×25 mL) and brine (2×20 mL), and dried over anhydrous Na2SO4. The solvent was removed in vacuo to afford 2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl ester (0.127 g, yield: 97%) as a dense oily liquid, which was used for the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449478B2
出典データセットuspto-grants-2008_11
ORD IDord-ac71b308e6764506acda086ceb619d3e
出典メモuspto-grants-2008_11