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HRID 30583作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-FluoroethanolHCID 9737—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物3-Bromobenzyl bromideHCID 69979—
溶媒TetrahydrofuranHCID 8028—
生成物1-Bromo-3-(2-fluoroethoxymethyl)benzeneHCID 1505877058%

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423158B2
出典データセットuspto-grants-2008_09
ORD IDord-158d176688544e6aa2e5b276473b5061
出典メモuspto-grants-2008_09