HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3,5-Bis(trifluoromethyl)anisole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Bis(trifluoromethyl)phenol | HCID 67680 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,5-Bis(trifluoromethyl)anisole | HCID 2737804 | 56.5% |
Reaction Steps
A mixture of 3,5-bis(trifluoromethyl)phenol (47, 1.0 g, 4.35 mmol), methyl iodide (0.7 mL, 10.8 mmol) and K2CO3 (3 g, 21.75 mmol) in acetone (10 mL) was heated to reflux while stirring overnight. Solid residue was filtered off and the filtrate was concentrated on warm water bath at atmospheric pressure (Caution: product was volatile) to afford 1-methoxy-3,5-bis(trifluoromethyl)benzene (48, 0.6 g, 56%) as clear oil: 1H NMR (300 MHz, CDCl3) δ 7.46 (s, 1H), 7.30 (s, 1H), 3.90 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045445B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-f043137f3bf645a1bf4ec5eb9de7efc0 |
| Source note | uspto-grants-2015_06 |