Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367311Generated: November 2, 2026

2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile → (4-Cyano-3,5-difluorophenyl)boronic acid

https://huagongshe.com/reaction/2367311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 58504590—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(4-Cyano-3,5-difluorophenyl)boronic acidHCID 5525291079%

Reaction Steps

2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (55 g) was dissolved in acetone (1 L) and water (1 L). T this stirred mixture was added NaIO4 (160 g) and NH4OAc (50 g). The reaction mixture was stirred at room temperature overnight and then filtered. The filtrate was evaporated under vacuum at 40° C. until most of acetone was removed. The residue was cooled to 0° C. and 2N NaOH (1 L) solution was added with stirring over 30 minutes. The mixture was filtered, and the filtrate was washed with CH2Cl2 (1 L). To the aqueous layer was added 5N hydrochloric acid at 0° C. until pH=2. The resulting solid was filtered and then dissolved in EtOAc (1.5 L), dried over Na2SO4, filtered and evaporated under vacuum to provide 30 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-b8b33cce66d0400b9126ec32f496a119
Source noteuspto-grants-2014_04