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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662916Generated: October 30, 2026

Hydrochloric Acid → 4-(6-Phenylnaphthalene-2-yl)phenylboronic acid

https://huagongshe.com/reaction/1662916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant2-(4-Bromophenyl)-6-phenylnaphthaleneHCID 57539811—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product4-(6-Phenylnaphthalene-2-yl)phenylboronic acidHCID 5753984763%

Reaction Conditions

Temperature-60 °C

Reaction Steps

Under an argon gas atmosphere, a mixture of 15.3 g (42.6 mmol) of 2-(4-bromophenyl)-6-phenylnaphthalene and 200 mL of dehydrated THF was cooled down to −60 degrees C., and added with 32.8 mL (51.1 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 degrees C. 24.0 g (128 mol) of triisopropyl borate was dropped into the reaction solution at −60 degrees C. Subsequently, the reaction mixture was warmed up to room temperature, and stirred for 17 hours. The reaction mixture was cooled down to 0 degree C. to be further added with solution of hydrochloric acid, and then 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 residue by toluene and hexane, 8.7 g of 4-(6-phenylnaphthalene-2-yl) phenylboronic acid was obtained at an yield of 63%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034256B2
Source datasetuspto-grants-2011_10
ORD IDord-f6e07d3117c74c41a6d7e7a2bf104804
Source noteuspto-grants-2011_10