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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480574생성일: 2026년 10월 24일

Nitrogen → 2-Methyl-3-trichloroacetyl-7-methoxyindole

https://huagongshe.com/ko/reaction/480574

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Trichloroacetyl chlorideHCID 6420—
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물7-methoxy-2-methyl-1H-indoleHCID 326614—
용매AcetonitrileHCID 6342—
생성물2-Methyl-3-trichloroacetyl-7-methoxyindoleHCID 18765417100.5%

반응 단계

To a 2 L round-bottomed flask equipped with a magnetic stirrer and a N2 bubbler were added 2-methyl-7-methoxyindole (12 g, 74 mmol), acetonitrile (125 mL) and collidine (15 mL, 113 mmol). The mixture was stirred to give a solution and was cooled with an ice water bath. Trichloroacetyl chloride (14 mL, 112 mmol) was added. The cooling bath was removed and the reaction mixture stirred at RT for 3 h. 1N HCl (500 mL) was then added over 10 minutes. The resulting slurry was stirred at RT for 30 minutes and filtered. The cake was washed with DI water (3×50 mL) and suction dried for 17 h to give 2-methyl-3-trichloroacetyl-7-methoxyindole (22.8 g, 96% yield). 1H NMR (CDCl3) δ2.79 (s, 3H), 3.96 (s, 3H), 6.71 (d, J=7.9 Hz, 1H), 7.19 (dd, J=7.9, 8.4 Hz, 1H), 7.82 (d, J=8.4 Hz, 1H), 8.92 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06653304B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-e61d8aad82694495aa717ba9557052fe
출처 메모uspto-grants-2003_11