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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2249373Erstellt: 24. Oktober 2026

Bromomethyl methyl ether → 1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzene

https://huagongshe.com/de/reaction/2249373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromomethyl methyl etherHCID 83093—
Edukt1-Bromo-4-chloro-2-fluorobenzeneHCID 137275—
EduktLithium diisopropylamideHCID 2724682—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzeneHCID 6880938171%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in THF (50 mL) was slowly added to LDA (0.125 mol) in THF (600 mL) at −50° C. After addition the solution was warmed to −20° C. and then cooled to −50° C. a solution of bromomethoxymethane (25 g, 0.200 mol) in THF (25 mL) was slowly added and the reaction mixture was warmed to ambient temperature. The reaction was quenched with water (400 mL) and extracted with diethyl ether (2×150 mL). The combined organic phases were dried (sodium sulfate) and concentrated. The residual oil was distilled (70°-75° C./0.5 mm) to give 1-bromo-4-chloro-2-fluoro-3-methoxymethylbenzene (18.0 g, 0.071 mol): 1H NMR (CDCl3): δ 7.50 (m, 1H), 7.15 (dd, 1H), 4.65 (s, 1H), 3.40 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07314849B2
Quelldatensatzuspto-grants-2008_01
ORD IDord-ac2da014daba480d85a8943209a2482b
Quellennotizuspto-grants-2008_01