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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347869Erstellt: 25. Oktober 2026

Trimethyl borate → 2,6-Dimethoxy-4-methoxymethylphenylboric acid

https://huagongshe.com/reaction/347869

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethyl borateHCID 8470—
EduktAmmonium ChlorideHCID 25517—
Edukt2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzeneHCID 23080940—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,6-Dimethoxy-4-methoxymethylphenylboric acidHCID 23080945—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

n-Butyllithium (2.64M hexane solution; 182 mL) was added dropwise to a solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene (121.3 g) in tetrahydrofuran (730 mL) at −78° C., and the mixture was stirred for 20 minutes. A solution of trimethoxyborane (61.7 mL) in tetrahydrofuran (20 mL) was then added to the reaction mixture at −78° C. When internal temperature was raised to −10° C., to the reaction mixture was added saturated aqueous ammonium chloride (730 mL), and stirring was continued for 15 minutes. The obtained reaction mixture was extracted with ethyl acetate, the extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (90.4 g) was obtained as a white solid from the n-hexane:ethyl acetate (2:3) fraction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176216B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-98cd5e7682ec4cf5b59bbbfda0652f27
Quellennotizuspto-grants-2007_02