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HRID 434020생성일: 2026년 10월 26일

Sodium hydride → 5-Allyloxy-1-[(6-chlorobenzo[1,3]dioxol-5-yl)methyl]-1h-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/434020

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물6-Chloropiperonyl chlorideHCID 90113—
반응물Ethyl 5-[(prop-2-en-1-yl)oxy]-1H-indole-2-carboxylateHCID 13286893—
촉매Tetrabutylammonium IodideHCID 67553—
용매DimethylformamideHCID 6228—
생성물5-Allyloxy-1-[(6-chlorobenzo[1,3]dioxol-5-yl)methyl]-1h-indole-2-carboxylic acid ethyl esterHCID 7003291043%

반응 단계

To a mixture of NaH (60% suspension in mineral oil, 0.24 g, 6.12 mmol) and DMF (20 mL) was added 5-allyloxyindole-2-carboxylic acid ethyl ester (1.0 g, 4.08 mmol), from Example 1(d). After stirring at room temperature for 1 h, 6-chloropiperonyl chloride (0.84 g, 4.08 mmol) was added followed by the addition of tetrabutyl ammonium iodide (0.15 g, 0.41 mmol). The reaction was stirred at room temperature for 18 h. When the reaction was complete as indicated by TLC, the reaction mixture was partitioned between EtOAc and water. The organic layer was washed with brine and dried (Na2SO4). The solvent was removed in vacuo and the resulting crude product was purified by flash column chromatography (silica gel, EtOAc/hexanes) to yield the desired product as an oil (0.72 g, 43%). LC/MS (ES+) m/e 414.0 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06670388B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-b1232f5cd63a4771b76d4c4fa67413d4
출처 메모uspto-grants-2003_12