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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41060생성일: 2026년 10월 27일

Hydrochloric Acid → [5-(2-methoxy-ethoxy)-1H-indol-ylmethyl]-dimethyl-amine

https://huagongshe.com/reaction/41060

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylamineHCID 674—
반응물FormaldehydeHCID 712—
반응물5-(2-methoxyethoxy)-1H-indoleHCID 10352537—
용매Acetic AcidHCID 176—
생성물[5-(2-methoxy-ethoxy)-1H-indol-ylmethyl]-dimethyl-amineHCID 6693846690%

반응 단계

A solution of 5-(2-methoxy-ethoxy)-indole (2.06 g, 11.0 mmol) in acetic acid (7 ml) and 40% aqueous dimethylamine (2.1 ml) is cooled to 0° C., and 36% aqueous formaldehyde (1.38 ml) (pre-cooled to 0° C.) is added drop wise. The mixture is stirred at room temperature overnight, 2 M hydrochloric acid is added, and the mixture is washed with dichloromethane. The aqueous layer is made alkaline with 10% NaOH, and is extracted with dichloromethane. The combined organic layer is washed with water, is dried and concentrated. The residue is purified by column chromatography (dichloromethane-methanol, 4:1→dichloromethane-methanol-water-aqueous ammonia, 10:20:1:1) to afford [5-(2-methoxy-ethoxy)-1H-indol-ylmethyl]-dimethyl-amine (2.42 g, 90%). M.p. 163-164° C. (from toluene-N,N-dimethylformamide).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530493B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-647412664e524dd98d16f3f196ff2ed6
출처 메모uspto-grants-2013_09