Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301487Generated: October 30, 2026

Hydrochloric Acid → 4-Cyanophenylboronic acid

https://huagongshe.com/reaction/2301487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzonitrile, 4-bromo-HCID 12162—
ReactantTriisopropyl borateHCID 21531—
ReactantButyllithiumHCID 178418339—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Cyanophenylboronic acidHCID 273432625%

Reaction Steps

A solution of 10.0 g (54.9 mmol) of 4-bromobenzonitrile in 100 mL of tetrahydrofuran was cooled to −85° C. whereupon 36.0 mL (57.6 mmol) of 1.6 M solution of n-butyllithium in hexane was added. The mixture was stirred for five minutes and 19.0 mL (82.4 mmol) of triisopropylborate was added. The mixture was stirred at −85° C. for 30 minutes then warmed to ambient temperature over one hour. To the mixture was added 35 mL of 5 N hydrochloric acid and stirring was continued for 2.5 hours. The mixture was diluted with 100 mL of saturated aqueous sodium chloride and extracted three times with 100 mL each of ethyl ether. The combined organics were dried (MgSO4), filtered and concentrated in vacuo. The residue was recrystallized from water and filtered to afford 2.0 g (25%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500865B1
Source datasetuspto-grants-2002_12
ORD IDord-b67dcf745d6f4d058e7ef1d9bd27ac14
Source noteuspto-grants-2002_12