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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15061Erstellt: 24. Oktober 2026

Chloromethyl Methyl Ether → 4-Fluoro-3-(methoxymethoxy)benzyl alcohol

https://huagongshe.com/de/reaction/15061

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloromethyl Methyl EtherHCID 7864—
EduktTetrahydrofuranHCID 8028—
EduktTriethylamineHCID 8471—
Edukt4-Fluoro-3-hydroxybenzoic acidHCID 593635—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Fluoro-3-(methoxymethoxy)benzyl alcoholHCID 2307431194%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Triethylamine (1.07 mL) and methoxymethyl chloride (2.24 mL) were added to tetrahydrofuran (10 mL) solution of 4-fluoro-3-hydroxybenzoic acid (1.0 g), and stirred at 0° C. for 2 hours. Ethyl acetate was added to the reaction liquid which then was washed with water and saturated brine, dried over anhydrous magnesium sulfate, the solvent therein was concentrated under reduced pressure and the residue was dissolved in tetrahydrofuran (20 mL). Lithiumaluminium hydride (360 mg) was added, stirred at 0° C. for an hour, ethyl acetate was added and the insoluble matter was removed, followed by washing with saturated brine and drying over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the title compound (1.14 g, 94%) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732456B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b32e232e6caf496cb7414acd838cedd1
Quellennotizuspto-grants-2010_06