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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045299Generated: October 30, 2026

Hydrochloric Acid → 4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)

https://huagongshe.com/reaction/1045299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant1-(4-bromophenyl)naphthaleneHCID 11208338—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)HCID 4411939968.9%

Reaction Steps

Under an argon gas atmosphere, a mixture of 208.8 g (737.4 mmol) of 1-(4-bromophenyl)naphthalene and 2.1 L of dehydrated THF was cooled down to minus 60 degree C. Then, 567 ml (884.9 mmol) of hexane solution of 1.56M n-butyllithium was dropped into the mixture while the mixture was being stirred. The reaction mixture was further stirred at minus 60 degrees for 2 hours. 416 g (2.21 mol) of triisopropylborate was dropped into the reaction mixture at minus 60 degrees C. The reaction mixture was then 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. After the reaction, the reaction mixture was added with toluene, and aqueous phase thereof was eliminated. Then, organic phase thereof was dried with magnesium sulfate, and the solvent was distilled away under reduced pressure. By recrystallizing the obtained solid by toluene, 126 g of 4-(1-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-7ba21a6bd01f4f52814d5dca8b509f0c
Source noteuspto-grants-2013_10