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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1829969생성일: 2026년 10월 25일

Methyl iodide → 1-Methyl-indole-2,5-dicarboxylic acid diethyl ester

https://huagongshe.com/reaction/1829969

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물diethyl 1H-indole-2,5-dicarboxylateHCID 15629756—
용매DimethylformamideHCID 6228—
생성물1-Methyl-indole-2,5-dicarboxylic acid diethyl esterHCID 6755017997%

반응 단계

Sodium hydride (60%-suspension, 144 mg, 3.6 mmole) was added to a stirred solution of 1H-indole-2,5-dicarboxylic acid diethyl ester 16 (784 mg, 3.0 mmole) in dry DMF (15.0 ml) and kept at ambient temperature for 30 min. To a resulted reaction mixture MeI (280 μl, 4.5 mmol) was added and kept at ambient temperature for 16 hours and evaporated. The residue was suspended in AcOEt (100 ml) and washed with water (2×20 ml), 0.01 M HCl (3×20 ml) and brine (2×100 ml). The organic layer was dried over sodium sulfate and evaporated to give 800 mg (97%) of 1-methyl-indole-2,5-dicarboxylic acid diethyl ester 17 as a yellow oil. 1H-NMR (DMSO-d6): δ 8.45 (m, 1H, H-4, indole); 8.03 (m, 1H, H-6, indole); 7.40 (m, 1H, H-7, indole); 7.38 (s, 1H, H-3, indole); 4.40 (m, 4H, —OCH2CH3); 4.10 (s, 3H, NCH3, indole); 1.42 (m, 4H, —OCH2CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07064218B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-61dcb7c3946b4bbba3231add4d6b8067
출처 메모uspto-grants-2006_06