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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30583Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-FluoroethanolHCID 9737—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt3-Bromobenzyl bromideHCID 69979—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Bromo-3-(2-fluoroethoxymethyl)benzeneHCID 1505877058%

Reaktionsschritte

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]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423158B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-158d176688544e6aa2e5b276473b5061
Quellennotizuspto-grants-2008_09