HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (4-Fluorophenyl)methyl 2-{[(4-fluorophenyl)methyl]oxy}-5-(trifluoromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | 2-hydroxy-5-(trifluoromethyl)benzoic Acid | HCID 11117203 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (4-Fluorophenyl)methyl 2-{[(4-fluorophenyl)methyl]oxy}-5-(trifluoromethyl)benzoate | HCID 67107202 | — |
Reaction Steps
To a solution of 2-hydroxy-5-(trifluoromethyl)benzoic acid (may be prepared as described in Description 117; 2 g, 9.70 mmol) in acetone (50 ml) was added 1-(bromomethyl)-4-fluorobenzene (4.04 g, 21.35 mmol), potassium carbonate (4.02 g, 29.1 mmol) and the reaction was heated to reflux overnight. The mixture was filtered to remove the solid potassium carbonate. The solid was washed with acetone (50 ml). The organics were combined and evaporated under reduced pressure on a buchi to yield the title compound. The crude yellow oil was used directly without further purification. 4.1 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778939B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-9a0ed384c6be459896c48ef05a9bcfc3 |
| Source note | uspto-grants-2014_07 |