HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(Difluoroacetyl)-3-fluorophenyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2,2-Difluoro-1-(2-fluoro-4-hydroxyphenyl)ethan-1-one | HCID 86638492 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Difluoroacetyl)-3-fluorophenyl trifluoromethanesulfonate | HCID 87535561 | — |
Reaction Steps
To 2,2-difluoro-1-(2-fluoro-4-hydroxyphenyl)ethanone (39.0 g, 0.2 mol) and Et3N (20.7 g, 0.2 mol) in CH2Cl2 at 0° C. was added Tf2O (58 g, 0.2 mol) dropwise while keeping the temperature at 0° C. The ice-salt bath was removed, and when the temperature rose to 25° C., a solution of saturated NaHCO3 was added. The aqueous phase was extracted with CH2Cl2 and the combined extracts were dried over MgSO4, and concentrated, and the residue was purified by column chromatography (PE/EA 10:1) to afford 4-(difluoroacetyl)-3-fluorophenyl trifluoromethanesulfonate as an brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193228B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-a2147d2d735341b29b214571b9408de3 |
| Source note | uspto-grants-2012_06 |