HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254970Generated: October 25, 2026
Potassium Carbonate → 2-(2-Chloro-3-trifluoromethyl-phenoxy)-butyronitrile
https://huagongshe.com/reaction/1254970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 2-Chloro-3-(trifluoromethyl)phenol | HCID 2736601 | — |
| Reactant | 2-(Methanesulfonyloxy)-butyronitrile | HCID 15467691 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(2-Chloro-3-trifluoromethyl-phenoxy)-butyronitrile | HCID 68735070 | — |
Reaction Steps
A mixture of 2-(methanesulfonyloxy)-butyronitrile (204 mg, 1.25 mmol) (prepared following Marco et. al., Tetrahedron, 2000, 56, 2525-31) 2-chloro-3-trifluoromethylphenol (196 mg, 1.0 mmol) and potassium carbonate (172 mg, 1.25 mmol) in acetonitrile (5 ml) was stirred for 1 hour at 95° C. The mixture was shaken between tBuOMe and water and the ethereal phase dried with Na2SO4, filtered over a silicagel pad and evaporated to give as yellowish oil 2-(2-chloro-3-trifluoromethyl-phenoxy)-butyronitrile; 1H-NMR (CDCl3): 1.27 t, 3H, 2.20 m, 2H, 2.40 s, 3H, 4.78 t, 1H, 7.34, d, 1H; 7.39, t, 1H, 7.48 d, 1H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455663B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-2a187544f3ea4e37bd4d380196138f44 |
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| Source note | uspto-grants-2013_06 |
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