HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodoxybenzoic acid → 1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | 1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethanol | HCID 61644635 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-one | HCID 66957864 | 95.3% |
Reaction Steps
To a solution of 1-(4-bromo-2-fluorophenyl)-2,2,2-trifluoroethanol (1.09 g, 3.99 mmol) in ethyl acetate (30 mL) was added 2-iodoxybenzoic acid (2.28 g, 7.97 mmol). The reaction was heated to reflux overnight. The reaction was cooled to room temperature and diluted with heptanes (30 mL). The mixture was filtered through Celite and the filtrate was concentrated to give the title compound (1.03 g, 95%) as a pale yellow oil. 1H NMR (400 MHz, CDCl3, δ): 7.44 (dd, J=10.15, 1.56 Hz, 1H), 7.48 (m, 1H), 7.76 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181252B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-2640f2ca716a4496b7a81e253e79dbf7 |
| Source note | uspto-grants-2015_11 |