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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 341700Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-Bromo-2,6-diethylphenylboronic acid

https://huagongshe.com/reaction/341700

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTrimethyl borateHCID 8470—
Edukt5-Bromo-1,3-diethyl-2-iodobenzeneHCID 44891101—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Bromo-2,6-diethylphenylboronic acidHCID 5956266367,1%

Reaktionsbedingungen

Temperatur-75 °C

Reaktionsschritte

To a solution of 4-bromo-2,6-diethyl-1-iodobenzene (10 g, 0.029 mol) in tetrahydrofuran (100 ml) at −75° C. is added n-butyl lithium (1.6 M in hexanes, 22.2 ml, 0.035 mol) dropwise maintaining the temperature of the reaction mixture below −70° C. When the addition is complete the mixture is stirred at −75° C. for an additional 30 minutes and then trimethyl borate (17.98 g, 0.17 mol) is added dropwise. After the addition is complete the reaction is stirred at −75° C. for 1 hour, then allowed to come to room temperature and stirred for 2 hours, followed by cooling in an ice bath and acidification with 0.5 N aqueous hydrochloric acid. The mixture is extracted with ethyl acetate (3×300 ml) and the organic fractions are combined, washed with brine, dried over anhydrous sodium sulphate. The mixture is filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4-bromo-2,6-diethylphenylboronic acid (5 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895761B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-fe41789ee4ec4ab390ca352e62ff41a8
Quellennotizuspto-grants-2014_11