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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584302Generated: October 30, 2026

Hydrochloric Acid → (5-(Ethoxymethoxy)-2-ethylphenyl)boronic acid

https://huagongshe.com/reaction/584302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant1-Bromo-2-ethyl-5-ethoxymethoxybenzeneHCID 22345616—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(5-(Ethoxymethoxy)-2-ethylphenyl)boronic acidHCID 22345587—

Reaction Conditions

Temperature-78 °C

Reaction Steps

12 g (49 mmol) of 1-bromo-2-ethyl-5-ethoxymethoxybenzene are placed in 200 ml of dry THF in a round-bottomed flask and under a stream of nitrogen. The reaction medium is cooled to −78° C. and 23 ml (58 mmol) of 2.5M n-butyllithium in hexane are added dropwise. 20 minutes later, 13.6 ml (59 mmol) of triisopropyl borate are added slowly. Stirring is continued for 1 hour at −78° C. The mixture is then poured into a solution of water and hydrochloric acid and is then extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a mixture of heptane and ethyl acetate (50/50). After evaporating off the solvents, 6.7 g (65%) of the expected product are obtained in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924400B2
Source datasetuspto-grants-2005_08
ORD IDord-d6fd86ff902941e38ed4258c2270b3d2
Source noteuspto-grants-2005_08