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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096652Generated: November 1, 2026

Triisopropyl borate → (5-Cyano-2-methylphenyl)boronic acid

https://huagongshe.com/reaction/2096652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant3-Bromo-4-methylbenzonitrileHCID 14004840—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(5-Cyano-2-methylphenyl)boronic acidHCID 5321674327.8%

Reaction Steps

A stirred solution of 3-bromo-4-methylbenzonitrile (3.5 g, 17.86 mmol) in dry THF was added n-BuLi (10.71 mL) slution dropwise at −78° C., and the mixture was stirred for 15 minutes, followed by the addition of triisopropyl borate (6.71 g, 35.71 mmol) in one portion. The reaction flask was kept in a cooling bath for 30 min., and room temperature for 3 hours. The solvent was removed, and the residue was dissolved in ether. The solution was washed with 1N HCl solution and water, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by recrystallyzation from the mixture of CH2Cl2 and hexane to give 5-cyano-2-methylphenylboronic acid (800 mg, 20%). 1H-NMR (CDCl3 400 MHz): δ7.50-7.78 (m, 2H), 7.30 (d, 1H), 2.42 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-a0906f0842064cabbfeed715965f4c80
Source noteuspto-grants-2013_05