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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430749Generated: October 29, 2026

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

https://huagongshe.com/reaction/1430749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant3-Bromo-4'-chloro-4-ethylbiphenylHCID 59445905—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4'-Chloro-4-ethylbiphenyl-3-ylboronic acidHCID 59445927—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-Bromo-4′-chloro-4-ethylbiphenyl (10 g, 0.03 mol) is dissolved in tetrahydrofuran (250 ml), and the temperature is brought to −78° C. n-Butyllithium (1.33 molar solution in hexanes, 34.6 ml) is added dropwise over 30 minutes, maintaining the temperature at around −78° C. The reaction mixture is stirred for one and a half hours, then trimethylborate (4.9 g, 0.05 mol) is added dropwise and the reaction mixture is stirred for two hours. A solution of 2N aqueous hydrochloric acid (100 ml) is added dropwise, and once the addition is complete the mixture is stirred for two hours. The mixture is concentrated to remove most of the tetrahydrofuran, then diluted with water and extracted with diethyl ether. The organic extracts are washed with water and brine, combined, dried over anhydrous sodium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is further purified by column chromatography on silica gel, eluting with 7% ethyl acetate in hexane to give 4′-chloro-4-ethylbiphen-3-ylboronic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940913B2
Source datasetuspto-grants-2015_01
ORD IDord-725e0f28c1474f268a27cc45af8aeb8a
Source noteuspto-grants-2015_01