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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341681Generated: October 26, 2026

Hydrochloric Acid → 4'-Chloro-3-methylbiphen-4-ylboronic acid

https://huagongshe.com/reaction/341681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant4-Bromo-4'-chloro-3-methylbiphenylHCID 59450516—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4'-Chloro-3-methylbiphen-4-ylboronic acidHCID 5945049359.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl lithium (1.6 M solution in hexanes, 37.5 ml, 0.060 mol) is added dropwise to a solution of 4-bromo-4′-chloro-3-methylbiphenyl (11.5 g, 0.041 mol) in tetrahydrofuran (120 ml) at −78° C., under an atmosphere of nitrogen, and the mixture is stirred at −78° C. for 30 minutes. Trimethyl borate (27.4 ml, 0.245 mol) is added slowly at −78° C. and the mixture is stirred for 1 hr. The reaction mixture is allowed to warm to room temperature over 2-3 hours and then stirred at room temperature for 1 hr. 0.1N Aqueous hydrochloric acid (320 ml) is added and the mixture is stirred at room temperature overnight. The reaction mixture is extracted with ethyl acetate (3×300 ml) and the organic extracts are combined, dried with anhydrous sodium sulfate, filtered and the filtrate is concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4′-chloro-3-methylbiphen-4-ylboronic acid (6.0 g) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895761B2
Source datasetuspto-grants-2014_11
ORD IDord-f8491472caa346e185240b41242fb8b2
Source noteuspto-grants-2014_11