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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954180Generated: November 2, 2026

Hydrochloric Acid → 3-Benzyloxy-phenylboronic acid

https://huagongshe.com/reaction/1954180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
ReactantBoronic AcidHCID 61668—
Reactant1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Benzyloxy-phenylboronic acidHCID 2734313—

Reaction Conditions

Temperature-78 °C

Reaction Steps

The 3-benzyloxybromobenzene of formula IV is converted to the boronic acid derivative by dissolving in THF and adding one equivalent of n-butyllithium at -78° C. After stirring at -78° C. for approximately 30 minutes, one equivalent of triisopropyl borate is added and the reaction is slowly warmed to room temperature, followed by acidification with aqueous hydrochloric acid to give a 3-benzyloxybenzene boronic acid compound of formula V. ##STR7##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06121293
Source datasetuspto-grants-2000_09
ORD IDord-433d0e0a45f244bdb7b38e350b57949f
Source noteuspto-grants-2000_09