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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711093Generated: October 25, 2026

2-Iodoxybenzoic acid → 1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-one

https://huagongshe.com/reaction/711093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodoxybenzoic acidHCID 108794—
Reactant1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethanolHCID 61644635—
SolventEthyl AcetateHCID 8857—
Product1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-oneHCID 6695786495.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181252B2
Source datasetuspto-grants-2015_11
ORD IDord-2640f2ca716a4496b7a81e253e79dbf7
Source noteuspto-grants-2015_11