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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2425057생성일: 2026년 10월 25일

2-Bromo-3-methylthiophene → 2-(2-Methoxy-ethyl)-3-methyl-thiophene

https://huagongshe.com/reaction/2425057

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-3-methylthiopheneHCID 84314—
반응물Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)HCID 86977—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
생성물2-(2-Methoxy-ethyl)-3-methyl-thiopheneHCID 66857153—

반응 단계

A part of a solution containing 2-bromo-3-methylthiophene CAS14282-76-9 (1.5 g, 8.5 mmol) in dry diethyl ether was added drop-wise to a suspension of magnesium (308 mg, 12.7 mmol, 1.5 equiv.) in dry diethyl ether, until the mixture started to reflux. The remaining solution was added dropwise. A solution of toluene-4-sulfonic acid 2-methoxy-ethyl ester (2.9 g, 12.7 mmol, 1.5 equiv.) in dry diethyl ether was added dropwise at room temp., then the mixture was refluxed for two hours. After cooling down to room temp., the mixture was quenched with ammonium chloride solution saturated and extracted with tert. butylmethyl ether. The combined organic extracts were washed with water and brine, dried over magnesiumsulfate-dihydrate and purified on silica gel with eluent n-heptane and tert.butylmethyl ether. The title compound was obtained as light yellow oil: 490 mg, GC-MS (EI) M=156.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07964633B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-94455c993f8841428b257b3430f0d43c
출처 메모uspto-grants-2011_06