HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455322Generated: October 29, 2026
Potassium Iodide → 2-(2-Methyl-3-trifluoromethyl-phenoxy)-butyronitrile
https://huagongshe.com/reaction/455322
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Methanesulfonyloxy)-butyronitrile | HCID 15467691 | — |
| Reactant | 2-Methyl-3-(trifluoromethyl)phenol | HCID 20111698 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-(2-Methyl-3-trifluoromethyl-phenoxy)-butyronitrile | HCID 67017862 | — |
Reaction Steps
A mixture of 2-(methanesulfonyloxy)-butyronitrile (449 mg, 2.75 mmol), 2-methyl-3-trifluoromethylphenol (440 mg, 2.5 mmol), potassium carbonate (432 mg, 3.13 mmol) and potassium iodide (42 mg, 0.25 mmol) in acetonitrile (20 ml) was stirred overnight at 80° C. The mixture was shaken between tBuOMe and water, washed with NaCl (aq. satd) and the ethereal phase dried with MgSO4 and evaporated. The crude product was chromatographed on silica with EtOAc and hexane to give 2-(2-methyl-3-trifluoromethyl-phenoxy)-butyronitrile. 1H-NMR (CDCl3) 1.20 t, 3H; 2.15 dt, 2H; 2.36 s, 3H; 4.75, t, 2H; 7.17, d, 1H; 7.28, t, 1H; 7.37 d, 1H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497293B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-dbdf93172c13420ebc420505bb91342d |
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| Source note | uspto-grants-2013_07 |
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