Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 1-{4-[3-(Trifluoromethyl)phenoxy]phenyl}ethan-1-one | HCID 12531831 | — |
| Reactant | HCID 18700168 | HCID 18700168 | — |
| Product | HCID 12531836 | HCID 12531836 | — |
Reaction Steps
A solution of 73.5 ml of 70% perchloric acid in 370 ml of methanol is cooled to 0° C and 73.76 g of thallium nitrate trihydrate followed by 42.25 g of 4'-(α,α,α-trifluoro-m-tolyloxy)acetophenone are added. The mixture is allowed to stir overnight while warming to room temperature. A white solid is rmoved by filtration and the filtrate is diluted with one liter of water. The resulting mixture is extracted with three 200 ml portions of chloroform. The combined organic extracts are washed with two 200 ml portions of water, 200 ml of saturated NaHCO3, saturated NaCl and dried over MgSO4. Evaporation of the solvent affords a yellow oil, which is filtered through aluminum oxide (benzene) and distilled at 0.07 mm to give the product as a yellow oil, bp 120°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04125729 |
|---|
| Source dataset | uspto-grants-1978_11 |
|---|
| ORD ID | ord-0f262ce447f140a18a70c91de156b6cb |
|---|
| Source note | uspto-grants-1978_11 |
|---|