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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536165Generated: October 30, 2026

Triphenylphosphine → 5-[(2-Chloro-4-pyrimidinyl)ethynyl]-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrile

https://huagongshe.com/reaction/536165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant5-Ethynyl-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrileHCID 86697024—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTriphenylphosphine palladium dichlorideHCID 13169693—
SolventTetrahydrofuranHCID 8028—
Product5-[(2-Chloro-4-pyrimidinyl)ethynyl]-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrileHCID 86697025—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of copper(I) iodide (117 mg, 0.613 mmol), dichloropalladium-triphenylphosphane (1:2) (215 mg, 0.306 mmol), 2,4-dichloropyrimidine (913 mg, 6.13 mmol), and 5-ethynyl-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrile (880 mg, 3.06 mmol) in a mixed solvents of TEA (18 mL, 129 mmol) and tetrahydrofuran (12 mL), was added triphenylphosphine (161 mg, 0.613 mmol) under Argon. The reaction mixture was stirred for 12 h at 60° C., filtered, washed with EA, concentrated. Purification via ISCO system (EtOAc=1:20 to 1:5) afforded the title compound as a brown solid. LC-MS (ESI): m/z 400 [M+H]+; 3.86 min (ret time).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859573B2
Source datasetuspto-grants-2014_10
ORD IDord-230ad4f9db334578a1e8691785ff5ace
Source noteuspto-grants-2014_10