Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727185Generated: October 30, 2026

Iodine → 1-Iodo-3,5-bis(trifluoromethyl)benzene

https://huagongshe.com/reaction/727185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
Reactant1-Bromo-3,5-bis(trifluoromethyl)benzeneHCID 67602—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Iodo-3,5-bis(trifluoromethyl)benzeneHCID 63097075.5%

Reaction Steps

Under a nitrogen atmosphere, a stirred solution of 15.0 grams (0.051 mole) of 3,5-di(trifluoromethyl)phenyl bromide in 45 mL of dry tetrahydrofuran was cooled to below -80° C., and 20.5 mL (0.051 mole) of n-butyllithium (2.5M in hexanes) was added dropwise while maintaining the reaction mixture temperature below -80° C. Upon completion of addition, an additional 50 mL of tetrahydrofuran was added to promote stirring. The reaction mixture was then stirred at -80° C. for an additional one hour. After this time a solution of 13.0 grams (0.051 mole) of iodine in 30 mL of tetrahydrofuran was added dropwise while maintaining the reaction mixture temperature below -80° C. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature. The reaction mixture was then poured into 400 mL of water, and the mixture was extracted with one 200 mL portion of diethyl ether. The ether extract was washed with an aqueous solution of 10% meta-sodium bisulfate. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 13.1 grams of 3,5-di(trifluoromethyl)phenyl iodide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712281
Source datasetuspto-grants-1998_01
ORD IDord-8872246719924cf5859b7042ea0781cf
Source noteuspto-grants-1998_01