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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045293Generated: October 29, 2026

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

https://huagongshe.com/reaction/1045293

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

Temperature78 °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 minus 10 degree C., and 600 ml (948 mmol) of hexane solution of 1.6M n-butyllithium was dropped into the mixture while the mixture was being stirred. Then, the mixture was stirred at 0 degree C. for 2 hours. The reaction solution was again cooled down to minus 78 degrees C., and 450 g (2.39 mol) of triisopropylborate was dropped into the solution. Then, the solution was stirred at room temperature for 17 hours. The reaction mixture was added with aqueous solution of hydrochloric acid and stirred at room temperature for 1 hour. The reaction mixture was added with 3 L of toluene, and 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 numberUS08568903B2
Source datasetuspto-grants-2013_10
ORD IDord-6957a9d711534eab8cd404aff147b96f
Source noteuspto-grants-2013_10