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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662911Generated: October 25, 2026

Hydrochloric Acid → 2-(9-Phenanthrenyl)naphthalene-6-boronic acid

https://huagongshe.com/reaction/1662911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant6-Bromo-2-(9-phenanthrenyl)naphthaleneHCID 57539827—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product2-(9-Phenanthrenyl)naphthalene-6-boronic acidHCID 5753980958%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Under an argon gas atmosphere, a mixture of 9.80 g (25.6 mmol) of 6-bromo-2-(9-phenanthrenyl)naphthalene, 100 mL of dehydrated toluene and 100 mL of dehydrated diethylether was cooled down to −10 degrees C., and added with 19.7 mL (30.7 mmol) of hexane solution of 1.56M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for four hours at −10 degree C. The reaction mixture was further cooled down to −60 degrees C., and added with 14.4 g (76.7 mmol) of triisopropyl borate in drops. The reaction mixture was subsequently warmed up to room temperature, and stirred for 16 hours at room temperature. The reaction mixture was further added with solution of hydrochloric acid to be stirred for one night at room temperature. After the reaction, the reaction mixture experienced liquid separation, organic phase thereof was cleansed with water, and the solvent was distilled away under reduced pressure until the reaction mixture became slurry. By adding residue thereof with hexane, filtering the solid and recrystallizing the residue by THF and hexane, 5.20 g of 2-(9-phenanthrenyl)naphthalene-6-boronic acid was obtained at an yield of 58%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034256B2
Source datasetuspto-grants-2011_10
ORD IDord-c5d9b747bcbc44138bcb20e6188205b6
Source noteuspto-grants-2011_10