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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912396Generated: October 30, 2026

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

https://huagongshe.com/reaction/912396

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 Conditions

Temperature-60 °C

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 −60 degrees C., and added with 567 mL (884.9 mmol) of hexane solution of 1.56M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for two hours at −60 degree C. 416 g (2.21 mol) of triisopropyl borate was dropped into the reaction solution at −60 degrees C. 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. After the reaction, the reaction mixture was further added with 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 4-(1-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-5669aff797644dc48cfc93f849cbb28e
Source noteuspto-grants-2011_09