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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250270생성일: 2026년 10월 26일

Methyl iodide → (6-benzyloxy-1-methyl-1H-indol-3-yl)-oxo-acetic acid methyl ester

https://huagongshe.com/reaction/250270

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물(6-Benzyloxy-1H-indol-3-yl)-oxo-acetic acid methyl esterHCID 34181007—
용매DimethylformamideHCID 6228—
생성물(6-benzyloxy-1-methyl-1H-indol-3-yl)-oxo-acetic acid methyl esterHCID 6727299024.1%

반응 조건

온도0 °C

반응 단계

A 0° C. suspension of (6-benzyloxy-1H-indol-3-yl)-oxo-acetic acid methyl ester (2.70 g, 8.73 mmol) in dimethylformamide (25 mL) is treated with sodium hydride (437 mg, 10.9 mmol). The mixture is stirred at 0° C. for 20 minutes. Methyl iodide (1.00 mL; 16.1 mmol) is added. The reaction mixture is stirred at 0° C. for 30 minutes and quenched with water (100 mL). The mixture is extracted with EtOAc (50 mL×2). The combined organic layers are dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product is purified by flash chromatography eluting with 60% EtOAc/Hexanes. The appropriate fractions are combined and concentrated under reduced pressure to afford the title compound (0.68 g, 24%). ES.MS m/e 324.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863302B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-1f922edc966447e9852169d0bed6bd28
출처 메모uspto-grants-2011_01