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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912392Generated: November 1, 2026

Hydrochloric Acid → [3-(Naphthalen-2-yl)phenyl]boronic acid

https://huagongshe.com/reaction/912392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant2-(3-Bromophenyl)naphthaleneHCID 23080773—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product[3-(Naphthalen-2-yl)phenyl]boronic acidHCID 4538225567.9%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Under an argon gas atmosphere, a mixture of 212 g (748 mmol) of 2(3-bromophenyl) naphthalene and 3 L of dehydrated THF was cooled down to −10 degrees C., and added with 600 ml (948 mmol) of hexane solution of 1.6M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for two hours at 0 degree C. The reaction solution was further cooled down to −78 degrees C., and added with 450 g (2.39 mol) of triisopropyl borate in drops. Subsequently, the reaction mixture was stirred for 17 hours at room temperature. The reaction mixture was further added with solution of hydrochloric acid to be stirred for one hour at room temperature. The reaction mixture was further added with 3 L of toluene, so that aqueous phase thereof was eliminated. After organic phase thereof was dried with magnesium sulfate, the solvent was distilled away under reduced pressure. By recrystallizing the obtained solid by toluene, 126 g of 3-(2-naphthyl) phenylboronic acid was obtained at an yield of 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08025815B2
Source datasetuspto-grants-2011_09
ORD IDord-13af4ed133344e998a5e121307500be5
Source noteuspto-grants-2011_09