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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7462생성일: 2026년 10월 23일

Water → 5-[2-(3-Bromopropoxy)ethyl]-1-benzothiophene

https://huagongshe.com/ko/reaction/7462

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Carbon tetrabromideHCID 11205—
반응물TriphenylphosphineHCID 11776—
반응물3-[2-(1-Benzothiophen-5-yl)ethoxy]-1-propanolHCID 21990066—
용매DichloromethaneHCID 6344—
생성물5-[2-(3-Bromopropoxy)ethyl]-1-benzothiopheneHCID 2199007676.2%

반응 단계

In 40 mL of methylene chloride was dissolved 2.00 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]-1-propanol, and 5.55 g of triphenylphosphine was added to the solution, after which a solution of 8.42 g of carbon tetrabromide in 10 mL of methylene chloride was added dropwise thereto under ice-cooling and the resulting mixture was stirred at room temperature for 20 minutes. To the reaction mixture was added 20 mL of water, and the organic layer was separated. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. Diethyl ether was added to the residue and the insoluble materials were filtered off, after which the solvent was distilled off under reduced pressure. The residue was purified by a column chromatography (eluent; hexane:ethyl acetate=20:1 to 10:1) to obtain 1.93 g of 5-[2-(3-bromopropoxy)ethyl]-1-benzothiophene as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087594B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-955645a8fc6a4fd1b0144ff9ec621f18
출처 메모uspto-grants-2006_08