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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252339생성일: 2026년 10월 23일

Water → 6-Bromo-1-(3-methoxypropyl)-1H-indole

https://huagongshe.com/ko/reaction/252339

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물1-Chloro-3-methoxypropaneHCID 118927—
반응물6-BromoindoleHCID 676493—
촉매Tetrabutylammonium IodideHCID 67553—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물6-Bromo-1-(3-methoxypropyl)-1H-indoleHCID 23151674—

반응 단계

The stirred solution of 25 g of 6-bromo-1H-indole [52415-29-9] in 250 ml of DMPU is admixed at 0° C. with 11.2 g of sodium hydride (60% in mineral oil) in portions. The mixture is stirred over 1 hour and then admixed with 60.9 g of 1-chloro-3-methoxypropane and 4.71 g of tetrabutylammonium iodide (exothermic reaction). The mixture is stirred at room temperature over a further 1 hour. The resulting reaction mixture is poured onto 2 l of water (cold) and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed successively with water (3×) and brine, dried over sodium sulphate and filtered, and the filtrate is concentrated by evaporation. The title compound is obtained as a slightly yellowish oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.31 (1:2 EtOAc-heptane). Rt=5.10 (gradient I).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868036B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-42a46c7ffb3e47b4bddaa7ddde6dc90d
출처 메모uspto-grants-2011_01