Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064751Generated: October 29, 2026

Sodium Carbonate → 2-fluoro-4-(4-methoxyphenyl)benzonitrile

https://huagongshe.com/reaction/1064751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
Product2-fluoro-4-(4-methoxyphenyl)benzonitrileHCID 276335792%

Reaction Steps

A mixture of 4-methoxyphenylboronic acid (4.56 g, 30.0 mmol) in ethanol (20 mL) was added to a solution of 4-bromo-2-fluorobenzonitrile (5.00 g, 25.0 mmol) and tetrakis(triphenylphosphine)palladium (578 mg, 0.50 mmol) in benzene (50 mL). The resulting mixture was treated with a 2.0 M aqueous solution of Na2CO3 (25 mL, 50 mmol) and heated briefly at reflux, then at 65° C. overnight. The mixture was cooled to room temperature and treated with 6.0 M aqueous NaOH. The aqueous phase was separated and extracted with ether. First the original organic phase and then the ethereal wash were filtered through diatomaceous earth. The collection flask was changed and the solids remaining atop the diatomaceous earth were washed through with EtOAc. The ethereal wash was concentrated and refiltered as before. The combined EtOAc rinses were combined and concentrated to provide the title compound as a yellow powder (92% yield). 1HNMR (300 MHz, d6-DMSO) δ 3.82 (s, 3 H), 7.07 (d, 2 H), 7.72 (dd, 1 H), 7.79 (d, 2 H), 7.85 (dd, 1 H), 7.95 (dd, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969730B2
Source datasetuspto-grants-2005_11
ORD IDord-0f5ad488e85b4af98df0f5d39e2a8c4f
Source noteuspto-grants-2005_11