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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045295Generated: October 31, 2026

Hydrochloric Acid → 4-(2-Naphthyl)phenylboronic Acid

https://huagongshe.com/reaction/1045295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant2-(4-Bromophenyl)naphthaleneHCID 5461752—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Naphthyl)phenylboronic AcidHCID 4538225884%

Reaction Steps

Under an argon gas atmosphere, a mixture of 50.0 g (177 mmol) of 2(4-bromophenyl)naphthalene and 500 mL of dehydrated THF was cooled down to minus 60 degree C. Then, 136 ml (212 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 1 hour. 99.6 g (529 mmol) of triisopropylborate was dropped into the reaction mixture at minus 60 degrees C. Subsequently, the reaction mixture was warmed up to room temperature, and stirred for 18 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, 33.6 g of 4-(2-naphthyl)phenylboronic acid was obtained at an yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08568903B2
Source datasetuspto-grants-2013_10
ORD IDord-f71c4560e16645bc8e0eb9d41471bfa9
Source noteuspto-grants-2013_10