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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660665Generated: October 31, 2026

Hydrochloric Acid → (4-(Phenanthren-9-yl)phenyl)boronic acid

https://huagongshe.com/reaction/1660665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant9-(4-Bromophenyl)phenanthreneHCID 23148610—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(4-(Phenanthren-9-yl)phenyl)boronic acidHCID 5757295772.4%

Reaction Conditions

Temperature-60 °C

Reaction Steps

Under an argon gas atmosphere, a mixture of 21.3 g (63.9 mmol) of 9-(4-bromophenyl)phenanthrene and 200 mL of dehydrated THF was cooled down to −60 degrees C., and added with 49.2 mL (76.7 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. The reaction solution was further cooled down to −60 degrees C. and added with 36.1 g (192 mol) of triisopropyl borate in drops. 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, 13.8 g of 4-(9-phenanthrenyl)phenylboronic acid was obtained at an yield of 72%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08029697B2
Source datasetuspto-grants-2011_10
ORD IDord-83cf22de5eae44bd962548ea825fad60
Source noteuspto-grants-2011_10