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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10070Generated: October 27, 2026

Water → Methyl 4'-Cyano[1,1'-biphenyl]-2-carboxylate

https://huagongshe.com/reaction/10070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 2-iodo-, methyl esterHCID 69132—
Reactant4-Cyanophenylboronic acidHCID 2734326—
CatalystBis(tri-o-tolylphosphine)palladium(II) DichlorideHCID 10876480—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4'-Cyano[1,1'-biphenyl]-2-carboxylateHCID 2198894286%

Reaction Steps

To 500 mL of THF was added water (18.4 mL, 1.02 mol), potassium carbonate (70.5 g, 0.510 mol), methyl 2-iodobenzoate (53.5 g, 0.204 mol), 4-cyano-phenylboronic acid (30.0 g, 0.204 mol) and bis-(tri-o-tolylphosphine) palladium (II) chloride (1.65 g, 2.04 mmol). This mixture was heated to reflux for 3.5 hours and then cooled to ambient temperature for continued stirring overnight. The solvent was then removed under reduced pressure prior to dilution with EtOAc/water. The organic layer was extracted with additional EtOAc. The combined organics were washed with water, then brine. The organics were then dried over sodium sulfate, filtered, and then concentrated to obtain the crude product. This crude product was passed through a silica pad, eluting with 8:1 heptane:EtOAc to get 41.6 grams of methyl 4′-cyano-1,1′-biphenyl-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091380B2
Source datasetuspto-grants-2006_08
ORD IDord-5ae0c0d393cb48bfbc9062688fae2658
Source noteuspto-grants-2006_08