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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272655Generated: November 1, 2026

1-Bromo-4-(trifluoromethoxy)benzene → HCID 59837911, compound

https://huagongshe.com/reaction/272655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
Reactant(3-Bromophenyl)-1H-imidazol-2-ylmethanoneHCID 3418429—
ReactantMagnesiumHCID 5462224—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 59837911HCID 5983791181%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of magnesium (0.644 g, 87.7 mmol) in THF (13 mL) at 50° C. is treated dropwise with a solution of 1-bromo-4-(trifluoromethoxy)benzene (6.32 g, 26.2 mmol) in THF over a period of 5 min, stirred at 50° C. for an additional 1.5 h, cooled to room temperature, treated with copper(I) iodide (0.041 g, 0.215 mmol) and a solution of 2-(3-bromobenzoyl)-1H-imidazole (2.60 g, 10.4 mmol) in THF, heated at 65° C. overnight, cooled to room temperature and diluted with a 1:1:1 mixture of ethyl acetate, water and saturated aqueous ammonium chloride. The phases are separated and the aqueous phase is extracted with ethyl acetate. The combined organic extracts are dried over sodium sulfate, filtered and concentrated. The resultant residue is purified by flash chromatography (silica, 85:15 to 75:25 hexanes/ethyl acetate as eluent) affords the title product as a yellow solid, 3.47 g (81% yield), identified by NMR and mass spectral analyses. 1H NMR (500 MHz, CDCl3) δ 8.98 (br s, 1H), 7.55 (t, J=1.6 Hz, 1H), 7.45 (dt, J=8.1, 1.9 Hz, 1H), 7.37-7.34 (m, 2H), 7.24-7.20 (m, 2H), 7.18 (d, J=8.1 Hz, 2H), 7.07 (br s, 1H), 6.98 (br s, 1H), 4.30 (br s, 1H); ESI MS m/z 412 [C17H12BrF3N2O2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456186B2
Source datasetuspto-grants-2008_11
ORD IDord-7fd60464afdc46a8b5acd44ed4909af3
Source noteuspto-grants-2008_11