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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429329Generated: October 30, 2026

Hydrochloric Acid → 2-(9-Phenanthrenyl)naphthalene-7-boronic acid

https://huagongshe.com/reaction/1429329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTriisopropyl borateHCID 21531—
Reactant7-Bromo-2-(9-phenanthrenyl)naphthaleneHCID 57540015—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-(9-Phenanthrenyl)naphthalene-7-boronic acidHCID 5854462885%

Reaction Conditions

Temperature-70 °C

Reaction Steps

In argon atmosphere, a liquid mixture of 12.27 (32.01 mmol) of 7-bromo-2-(9-phenanthrenyl)naphthalene and 130 ml of dry THF was cooled to −70° C., and 24.8 ml (38.4 mmol) of a 1.56 M hexane solution of n-butyllithium was added dropwise under stirring. Further, the reaction mixture was stirred at −70° C. for 4 h. The reaction mixture was added dropwise with 18.06 g (96.04 mmol) of triisopropyl borate while maintaining the temperature at −60° C. or lower and then stirred for one hour. The reaction mixture was heated, stirred at room temperature for 3 h, and then allowed to stand overnight. The reaction mixture was added with 100 ml of a 6 N hydrochloric acid while maintaining the temperature at 20° C. or lower by cooling on an ice bath. The reaction mixture was stirred at room temperature for 30 min, added with dichloromethane, and then allowed to separate into liquid phases. The organic phase was washed with water and dried over anhydrous sodium sulfate. The solvent was removed by distillation to obtain 9.50 g (yield: 85%) of 2-(9-phenanthrenyl)naphthalene-7-boronic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940412B2
Source datasetuspto-grants-2015_01
ORD IDord-a6c504ab49ab46a6a2271d216e185e51
Source noteuspto-grants-2015_01