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HRID 341703Erstellt: 25. Oktober 2026

Hydrochloric Acid → (4-Bromo-2,6-dimethylphenyl)boronic acid

https://huagongshe.com/reaction/341703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTrimethyl borateHCID 8470—
Edukt5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4-Bromo-2,6-dimethylphenyl)boronic acidHCID 5749730143,7%

Reaktionsbedingungen

Temperatur-75 °C

Reaktionsschritte

To a solution of 4-bromo-2,6-dimethyl-1-iodobenzene (150 g, 0.48 mol) in tetrahydrofuran (1500 ml) at −75° C. is added n-butyl lithium (1.6 M in hexanes, 364 ml, 0.58 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 (302 g, 2.9 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 (3×1000 ml) and the organic extracts 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-dimethylphenylboronic acid (48 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895761B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-c6a1d681e830422eb8e2f8b1d14f81ac
Quellennotizuspto-grants-2014_11