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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1712204Erstellt: 27. Oktober 2026

Hydrochloric Acid → 3,5-Difluoro-4-(1-methylheptyloxy)phenylboronic acid

https://huagongshe.com/reaction/1712204

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTrimethyl borateHCID 8470—
Edukt5-Bromo-1,3-difluoro-2-[(octan-2-yl)oxy]benzeneHCID 68499982—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt3,5-Difluoro-4-(1-methylheptyloxy)phenylboronic acidHCID 68499248—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

14.5 g of 1-bromo-3,5-difluoro-4-(1-methylheptyloxy)benzene from step 1 were dissolved in 150 ml of diethyl ether and cooled to −70° C. At this temperature, with cooling, firstly 31.0 ml of a 15% solution of butyllithium in n-hexane were slowly added dropwise, the mixture was stirred at the same temperature for 1 h, and then 5.6 ml of trimethyl borate were slowly added dropwise, and the mixture was stirred for a further h. The temperature of the reaction solution was slowly allowed to rise to −10° C. The mixture was then hydrolysed with distilled water, and the pH was adjusted to 2 using hydrochloric acid. The organic phase was separated off, and the aqueous phase was extracted with MTB ether. The product was subjected to conventional purification and dried over Na2SO4, giving 13.9 g of 3,5-difluoro-4-(1-methylheptyloxy)phenylboronic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07790929B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-5af2f04a350c4adaabb2df1cab296330
Quellennotizuspto-grants-2010_09