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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269535Erstellt: 26. Oktober 2026

Hydrochloric Acid → 2'-Benzyloxy-biphenyl-2-boronic acid

https://huagongshe.com/reaction/269535

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriisopropyl borateHCID 21531—
EduktAcetone cardiceHCID 18522661—
Edukt2'-Benzyloxy-2-bromobiphenylHCID 58730989—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2'-Benzyloxy-biphenyl-2-boronic acidHCID 5873099080%

Reaktionsschritte

A solution of 2′-benzyloxy-2-bromobiphenyl (2.41 g, 7.09 mmol) in tetrahydrofuran (50 ml) was stirred under nitrogen and cooled to −100° C. (diethyl ether/liquid nitrogen). 1.6M nButyllithium in hexanes (4.87 ml, 7.80 mmol) was added over 15 mins. at −100° C. and the mixture warmed to −78° C. (acetone/Drikold) and stirred for 1 h. Triisopropyl borate (4.00 g (5.02 ml, 21.30 mmol) was added at −78° C. and the reaction allowed to warm to room temperature with stirring over 1.5 h. 1M Hydrochloric acid (50 ml) was added and the mixture stirred vigorously for 1 h. The organic layer was separated and the aqueous layer extracted with diethyl ether (50 ml). The combined organic phase were washed with water, dried (MgSO4) and the solvent removed in vacuo. The yellow oil was flash chromatographed (silica gel, 10-20% EtOAc-isohexane) to give the title compound as a clear oil (1.74 g, 80%). LC/MS RT=3.28 min [(2M−H2O)H−]=589.3

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07446222B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-212f4fc7464e40c4bd2bff88e26051d6
Quellennotizuspto-grants-2008_11