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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | 5-Ethynyl-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrile | HCID 86697024 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Triphenylphosphine palladium dichloride | HCID 13169693 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-[(2-Chloro-4-pyrimidinyl)ethynyl]-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrile | HCID 86697025 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859573B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-230ad4f9db334578a1e8691785ff5ace |
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| Source note | uspto-grants-2014_10 |
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