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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858580Generated: October 30, 2026

Sodium Carbonate → 3-(4-bromophenyl)benzonitrile

https://huagongshe.com/reaction/858580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant3-Cyanophenylboronic acidHCID 2734325—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product3-(4-bromophenyl)benzonitrileHCID 139385139.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a magnetically stirring solution of 3-cyanophenyl boronic acid (0.62 g, 4.24 mmol) and 1-bromo-4-iodobenzene (1.0 g, 3.53 mmol) in anhydrous DMF (7.0 mL), under argon at room temperature, was added 2M sodium carbonate solution (7.0 mL) followed by Pd(PPh3)4 (0.21 g, 0.18 mmol). The resulting mixture was heated to 75° C. overnight. The resulting dark reaction mixture was cooled to room temperature filtered to remove the solids and the resultant filtrate was poured into water (50 mL) and extracted with EtOAc (2×25 mL). The organics were washed with water (50 mL) and brine (50 mL) then dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (5% EtOAc in Hexanes) to yield the intermediate bromide as a white solid (0.36 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-d8598b58fe614d1f88edbdb94a781154
Source noteuspto-grants-2006_12