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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662356Generated: October 30, 2026

Potassium Phosphate, Tribasic → HCID 57706456, compound

https://huagongshe.com/reaction/1662356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Fluoro-5-methoxyphenylboronic acidHCID 4157211—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant4-Chloro-3-(trifluoromethoxy)benzaldehydeHCID 17750790—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 57706456HCID 5770645664%

Reaction Conditions

Temperature40 °C

Reaction Steps

A screw-cap vial was charged with 4-chloro-3-(trifluoromethoxy)benzaldehyde (available from Alfa Aesar, Avocado, Lancaster) (0.184 g, 0.82 mmol), 2-fluoro-5-methoxyphenylboronic acid (available from Aldrich) (0.278 g, 1.64 mmol), potassium phosphate (0.522 g, 2.46 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.101 g, 0.25 mmol), palladium(II) acetate (0.018 g, 0.082 mmol), and 5:1 THF/DMF (3.6 mL). The mixture was stirred overnight at 40° C., cooled to room temperature, diluted with EtOAc, washed with water and brine, dried (MgSO4), and concentrated. The crude product was chromatographed on silica gel (0-10% EtOAc/hexane) to afford 46.1 (165 mg, 64%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-3aee63ab0296439ba3827ba918c2b969
Source noteuspto-grants-2011_10