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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 617911Erstellt: 27. Oktober 2026

Boric acid (H3BO3), tripropyl ester → 3-Benzyloxy-phenylboronic acid

https://huagongshe.com/reaction/617911

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoric acid (H3BO3), tripropyl esterHCID 12711—
Edukt1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Benzyloxy-phenylboronic acidHCID 2734313—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

20 g (76 mmol) of 3-Benzyloxybromobenzene was dissolved in 200 mL of anhydrous THF and cooled to -78° C. under a nitrogen atmosphere. To the stirring solution, 90 mL of 1.6 M n-BuLi (83.6 mmol) was slowly added. After several minutes, 33.6 mL (83.6 mmol) tripropylborate was added and the reaction was allowed to slowly warm to ambient temperature over the next four hours. The reaction was quenched with the addition of 400 mL of 1N HCl. The reaction mixture was extracted three times with EtOAc. The EtOAc solution was washed twice with brine, dried with Na2SO4, and evaporated to dryness. The final product was crystallized from EtOAc-hexane. This yielded 10 g of the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05952350
Quelldatensatzuspto-grants-1999_09
ORD IDord-ed65f16852564c2d8ad36d1c1f88fc00
Quellennotizuspto-grants-1999_09