HuagongsheHuagongshe Chemistry Print Report · For research reference only
Antimony trifluoride → Methyl 3-methoxy-4-(trifluoromethoxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Antimony trifluoride | HCID 24554 | — |
| Reactant | Methyl 4-(bromodifluoromethoxy)-3-methoxybenzoate | HCID 71136603 | — |
| Catalyst | Antimony pentachloride | HCID 24294 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 3-methoxy-4-(trifluoromethoxy)benzoate | HCID 71136533 | 77.5% |
Reaction Conditions
| Temperature | 170 °C |
|---|
Reaction Steps
Antimony (V) Chloride (26.4 mg, 0.088 mmol) was added to a stirred, room temperature mixture of 173A (550 mg, 1.768 mmol) and antimony trifluoride (221 mg, 1.238 mmol) in a sealed tube, and the mixture was stirred at 170° C. for 4 h. The mixture was cooled, diluted with diethyl ether (50 mL), washed with water (50 mL), dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel; 24 g prepacked column, eluting with EtOAc/isohexane=10% to give methyl 3-methoxy-4-(trifluoromethoxy)benzoate 173B (240 mg, 0.959 mmol, 54.3% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592383B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-f55a0f17afa441148add2cc58971724b |
| Source note | uspto-grants-2013_11 |