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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28476생성일: 2026년 10월 24일

Methanol → 1-[(1-Benzhydryl-azetidin-3-yl)-methoxy-methyl]-5-fluoro-1H-indole

https://huagongshe.com/ko/reaction/28476

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium HydroxideHCID 14798—
반응물5-FluoroindoleHCID 67861—
반응물(1-Benzhydryl-azetidin-3-yl)-acetaldehydeHCID 58739272—
생성물1-[(1-Benzhydryl-azetidin-3-yl)-methoxy-methyl]-5-fluoro-1H-indoleHCID 2189204556%

반응 단계

A solution of (1-benzhydryl-azetidin-3-yl)-acetaldehyde (0.30 g, 1.2 mmol), 5-fluoroindole (0.8 g, 6.0 mmol) and sodium hydroxide (0.6 g, 1.6 mmol) in methanol (20 mL) was refluxed for 6 hours. The reaction was quenched with water and extracted with methylene chloride (3×100 mL). The organic layer was washed with water (3×80 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude oil was column chromatographed on silica gel (30-40% ethyl acetate/hexane). The product-containing fractions were concentrated under vacuum to give 0.27 g (56%) of the title compound as a light yellow oil. 1H NMR (500 MHz, DMSO-D6): δ 2.62 (t, J=6.4 Hz, 1H), 2.90-2.95 (m, 2H), 3.02 (t, J=6.1 Hz, 1H), 3.09 (s, 3H), 3.26-3.31 (m, 1H), 4.40 (br, 1H), 4.58 (d, J=8.8 Hz, 1H), 6.89 (m, 1H), 7.13-7.18 (m, 2H), 7.22-7.27 (m, 4H), 7.31-7.39 (m, 7H) 11.10 (br, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419986B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-519f8bb17ca34ccd9864ba4ba603d41c
출처 메모uspto-grants-2008_09