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HRID 384850作成日:2026年10月26日

CID 406 → 3-(5-Methoxy-1H-indol-3-yl)-acrylic acid methyl ester

https://huagongshe.com/reaction/384850

反応式

関与物質

役割名称HCID仕込み量
反応物CID 406HCID 406—
反応物Sodium hydrideHCID 24758—
反応物5-Methoxyindole-3-carbaldehydeHCID 82758—
反応物MethylacetylphosphonateHCID 170449—
反応物HCID 178418361HCID 178418361—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物3-(5-Methoxy-1H-indol-3-yl)-acrylic acid methyl esterHCID 5884308078%

反応条件

温度55 °C

反応手順

To a cold solution (ice bath) of methyl phosphonoacetate (13.74 g, 0.065 mol) in tetrahydrofuran (120 mL) under nitrogen, was added sodium hydride (2.6 g, 0.065 mol, 60%) in one portion, and stirred until hydrogen evolution ceased. A solution of commercially available 5-Methoxyindole-3-carboxyaldehyde 2 (5.2 g, 0.029 mol) in tetrahydrofuran (80 mL) was added, over a period of 60 minutes, to the phosphonate solution. The reaction mixture was heated to 55° C. for 24 h after which the mixture was diluted with dichloromethane (DCM, 500 mL) and washed with water (200 mL; 3×). The organic layer was washed once with brine, dried over anhydrous sodium sulfate, and evaporated under reduced pressure to give yellow-tinted oil and purified by filtering through a silica plug. The filtrate was evaporated to afford 3 as an off white solid (6.2 g; 78% yield; M+1=232.0).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367828B2
出典データセットuspto-grants-2013_02
ORD IDord-c933a81f547e4951912d2cacb86e7c1b
出典メモuspto-grants-2013_02