HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433193Generated: October 27, 2026
Sodium Iodide → 2-[4-(Trifluoromethyl)phenoxy]acetonitrile
https://huagongshe.com/reaction/1433193
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(Trifluoromethyl)phenoxy]acetonitrile | HCID 2777573 | 96.2% |
Reaction Steps
A mixture of 4-trifluoromethyl-phenol (25.0 g, 0.154 mol), bromoacetonitrile (12.9 mL, 0.185 mol), sodium carbonate (32.7 g, 0.308 mol), and sodium iodide (23.1 g, 0.154 mol) in 214 mL of DMF was heated at 100° C. for 2 hours. The reaction was cooled, and partitioned between water and EtOAc. The organic layers were washed with water and brine, dried with Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes:EtOAc, 4:1) to afford the title compound as a colorless oil (29.8 g, 96%). 1H NMR (400 MHz, CD3Cl) δ (ppm): 7.63 (d, 2H), 7.07 (d, 2H), 4.83 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612211B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-be1ef2b50e5d4b30ae8cae2cff284910 |
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| Source note | uspto-grants-2009_11 |
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