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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475143Generated: October 25, 2026

Iodopentafluoroethane → 1-Bromo-4-(pentafluoroethyl)benzene

https://huagongshe.com/reaction/1475143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodopentafluoroethaneHCID 9636—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant1-(4-Pentafluoroethylphenyl)-3-p-tolyl-1H-[1,2,4]triazoleHCID 86633385—
CatalystCopperHCID 23978—
SolventDimethyl SulfoxideHCID 679—
Product1-Bromo-4-(pentafluoroethyl)benzeneHCID 54209708—
Product1-Iodo-4-pentafluoroethylbenzeneHCID 86633384—

Reaction Steps

1-(4-Pentafluoroethyl-phenyl)-3-p-tolyl-1H-[1,2,4]triazole. Pentafluoroethyl iodide (521 mg, 2.12 mmol) was condensed into a vial containing 1-bromo-4-iodobenzene (300 mg, 1.06 mmol), copper(0) powder (135 mg, 2.12 mmol), and DMSO (5 mL). The vial was then sealed and subjected to microwave irradiation at 150° C. for 60 min GC/MS proved consumption of the starting material yielding both 1-bromo-4-pentafluoroethylbenzene and 1-iodo-4-pentafluoroethyl-benzene intermediates. The mixture (1.06 mmol), was transferred to a 250 mL round bottom flask and 3-p-tolyl-1H-[1,2,4]triazole (169 mg, 1.06 mmol), Cs2CO3 (1.38 g, 4.24 mmol), CuI (202 mg, 1.06 mmol), 8-hydroxyquinoline (2 mg, 0.011 mmol), and DMF/H2O (12 mL 10:1 solution) were added and the solution was refluxed at 160° C. for 6 h. Upon completion, the cooled contents were poured into H2O and precipitation was allowed for 1 h. The precipitate was collected by vacuum filtration and dried overnight in a 45° C. vacuum oven. The crude 1-(4-pentafluoroethylphenyl)-3-p-tolyl-1H-[1,2,4]triazole intermediate was used in step 2 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018363B2
Source datasetuspto-grants-2015_04
ORD IDord-803eb43c05a24e6cb9d9a24ea091a270
Source noteuspto-grants-2015_04