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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2195740생성일: 2026년 10월 26일

1,4-Dioxane → 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/2195740

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물4-Fluorobenzyl bromideHCID 68021—
반응물Methyl 1-methyl-1H-indole-5-carboxylateHCID 10679201—
용매Diethyl EtherHCID 3283—
생성물3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 6944955222%

반응 단계

A solution of 1-methyl-1H-indole-5-carboxylic acid methyl ester (0.17 g, 0.9 mmol), prepared using procedures as described in Example 1, Ag2O (0.22 g, 0.95 mmol), 4-fluoro-benzyl bromide (0.18 g, 0.95 mmol) and dioxane (4 mL) were heated to reflux for 16 hr, then more 4-fluoro-benzyl bromide (90 mg, 0.5 mmol) was added and the solution was heated at reflux an additional 4 hr. After cooling to room temperature, the reaction mixture was diluted with ether (60 mL), washed with aq. NH4Cl (50 mL) and then brine (50 mL). The organic layer was dried over MgSO4, filtered and concentrated. The remaining residue was subjected to flash chromatography (ethyl acetate/hexane, 1:3) to provide 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (58 mg, 22% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338416B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-191b2343760049c6955112d6e23c3b74
출처 메모uspto-grants-2012_12