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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393347Generated: November 2, 2026

Hydrochloric Acid → 6-Methoxy-2-naphthaleneboronic acid

https://huagongshe.com/reaction/1393347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTributyl borateHCID 12712—
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-2-naphthaleneboronic acidHCID 464169259%

Reaction Steps

A solution of n-butyl lithium in hexane (1.5M; 8.9 ml, 13.4 mmol) was added dropwise to a solution of 2-bromo-6-methoxynaphthalene (3.0 g, 12.7 mmol) in tetrahydrofuran (45 ml) under argon atmosphere at −60° C. and the mixture was stirred at the same temperature for 70 min. To the mixture was added tri-n-butylborate (5.2 ml, 19.0 mmol) and the mixture was stirred at the same temperature for 1 hr. and then at 5° C. for 1.5 hrs. To the reaction mixture was added dropwise 20% hydrochloric acid (13 ml) at 5° C., and water was added thereto. The mixture was extracted with ethyl acetate. The organic layer was washed with water and brine in turn and dried. The solvent was distilled off under reduced pressure, and the residue was triturated with ethyl acetate and diethyl ether, filtered and dried to give (2-methoxy)-6-naphthalene boronic acid (1.50 g, 59%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345068B2
Source datasetuspto-grants-2008_03
ORD IDord-ca504e7b04c24e9bb459ddab10f2f53f
Source noteuspto-grants-2008_03