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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30583생성일: 2026년 10월 23일

2-Fluoroethanol → 1-Bromo-3-(2-fluoroethoxymethyl)benzene

https://huagongshe.com/ko/reaction/30583

반응식

참여 물질

역할이름HCID투입량
반응물2-FluoroethanolHCID 9737—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물3-Bromobenzyl bromideHCID 69979—
용매TetrahydrofuranHCID 8028—
생성물1-Bromo-3-(2-fluoroethoxymethyl)benzeneHCID 1505877058%

반응 단계

A mixture of sodium hydride [60% in oil] (343, mg, 8.6 mmol) and THF at −5° C. was treated via a syringe with a solution of 2-fluoroethanol in THF over a 1 min. period, stirred for 2 min., warmed to room temperature, stirred for 15 min. at room temperature, treated with 3-bromobenzylbromide (2.5 g, 11.7 mmol), stirred for 1 h, poured into saturated ammonium chloride and extracted with ether. The extracts were combined, washed sequentially with water and brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel, 20:1 hexane/ ethyl acetate as eluent, to afford 1-bromo-3-(2-fluoroethoxymethyl)benzene as a yellow oil, 1 g (58% yield), 1H NMR (DMSO-d6) δ 3.6 (dxt, 2H); 4.5 (dxt, 2H); 4.4 (s, 2 H); 7.3 (m, 2H); 7.5 (m, 2H); MS [(+)ESI] m/z 219 [M−H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423158B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-158d176688544e6aa2e5b276473b5061
출처 메모uspto-grants-2008_09