Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72253Generated: October 28, 2026

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

https://huagongshe.com/reaction/72253

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 5944592769.1%

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 cooled 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 mole) 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 in vacuo. The residue is further purified by flash column chromatography on silica gel, eluting with 7% ethyl acetate in hexane to give 4′-chloro-4-ethylbiphen-3-ylboronic acid (5.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828908B2
Source datasetuspto-grants-2014_09
ORD IDord-a7a48e34eb3c402f9536a3f39d33fe63
Source noteuspto-grants-2014_09