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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909959Generated: October 30, 2026

Hydrochloric Acid → [3-(Naphthalen-1-yl)phenyl]boronic acid

https://huagongshe.com/reaction/909959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant3-(1-Naphthyl)-1-bromobenzeneHCID 22138047—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product[3-(Naphthalen-1-yl)phenyl]boronic acidHCID 5888107771.9%

Reaction Conditions

Temperature-60 °C

Reaction Steps

Under an argon gas atmosphere, a mixture of 200.0 g (706.3 mmol) of 1(3-bromophenyl)naphthalene and 2.1 L of dehydrated THF was cooled down to −60 degrees C., and added with 543 ml (847 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. 398.5 g (2.119 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 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 3-(1-naphthyl)phenylboronic acid was obtained at an yield of 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08021574B2
Source datasetuspto-grants-2011_09
ORD IDord-0f238e604f6e41a081bb9798db468472
Source noteuspto-grants-2011_09