HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466105Generated: November 4, 2026
Trifluoroacetic acid → 5-bromo-4-chloroisobenzofuran-1(3H)-one
https://huagongshe.com/reaction/1466105
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Reactant | Thallium(1+);2,2,2-trifluoroacetate | HCID 21902506 | — |
| Reactant | (3-Bromo-2-chlorophenyl)methanol | HCID 67146654 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-bromo-4-chloroisobenzofuran-1(3H)-one | HCID 67518202 | — |
Reaction Steps
To a flask charged with (3-bromo-2-chlorophenyl)methanol (1.1 g, 4.8 mmol) and a stir bar was added thallium trifluoroacetate (2.9 g, 5.3 mmol) and TFA (6 mL). The mixture was allowed to stir at RT for 16 hours. The volatiles were removed under reduced pressure. The residue was pumped under high vacuum for 15 minutes before palladium (II) chloride (0.085 g, 0.48 mmol), magnesium oxide (0.39 g, 9.6 mmol), lithium chloride (0.20 g, 4.8 mmol), and ethanol (30 mL) were added. The mixture was stirred under an atmosphere of carbon mono-oxide until the reaction turned black. The reaction was diluted with DCM. The suspension was filtered through a pad of celite to remove the solids. The filtrate was adsorbed onto silica gel, and purified by MPLC to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08999990B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-30eb990e374c49b5b729898c73a57836 |
|---|
| Source note | uspto-grants-2015_04 |
|---|