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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408846Generated: November 1, 2026

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

https://huagongshe.com/reaction/1408846

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

To a stirred solution of 3-bromo-4-methylbenzonitrile (3.5 g, 17.86 mmol) in dry THF at −78° C. was added n-BuLi (2N, 10.71 mL) dropwise. The mixture was stirred for 15 min., and added triisopropyl borate (6.71 g, 35.71 mmol). The reaction flask was kept in the cooling bath for 30 min., and at room temperature for 3 hours. The solvent was removed, and the residue was dissolved in ether. The organic phase was washed with 1N HCl solution and water, dried over Na2SO4, and filtered. The filtrate was concentrated in vacuo, and the residue was crystallized from a 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 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-3dac17cb61f345ce8566a08aa68f6b88
Source noteuspto-grants-2014_12