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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537172Generated: October 25, 2026

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

https://huagongshe.com/reaction/537172

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 numberUS08859773B2
Source datasetuspto-grants-2014_10
ORD IDord-89405abb30dc4596aa617a820cba13eb
Source noteuspto-grants-2014_10