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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341694Generated: October 31, 2026

Hydrochloric Acid → 4'-Chloro-3,5-diethylbiphen-4-ylboronic acid

https://huagongshe.com/reaction/341694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant4-Bromo-4'-chloro-3,5-diethylbiphenylHCID 59450488—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product4'-Chloro-3,5-diethylbiphen-4-ylboronic acidHCID 5945050144.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

tert-Butyllithium (1.6 M solution in hexanes, 13 ml, 0.02 mol) is added dropwise to a solution of 4-bromo-4′-chloro-3,5-diethylbiphenyl (4.5 g, 0.0139 mol) in dry tetrahydrofuran (50 ml) at −78° C. under an atmosphere of nitrogen. The reaction mixture is stirred at −78° C. for 30 minutes, then trimethylborate (9.3 ml, 0.083 mol) is added. The resulting mixture is stirred at −78° C. for 1 hour and then allowed to warm to room temperature over 3 hours. The reaction mixture is acidified with 0.1 N aqueous hydrochloric acid solution and the mixture is stirred at room temperature overnight. The mixture is extracted with ethyl acetate (3×100 ml). The organic layers are combined, dried over anhydrous sodium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4′-chloro-3,5-diethylbiphen-4-ylboronic acid as a white powder (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895761B2
Source datasetuspto-grants-2014_11
ORD IDord-ba0f4ec621994be79ca8b591de6939f6
Source noteuspto-grants-2014_11