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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847102Generated: October 25, 2026

Pentafluoroiodobenzene → 2,3,4,5,6-Pentafluoro-2'-methoxy-5'-methyl-1,1'-biphenyl

https://huagongshe.com/reaction/1847102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentafluoroiodobenzeneHCID 70008—
Reactant2-(2-Methoxy-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 79662121—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventPotassium CarbonateHCID 11430—
Product2,3,4,5,6-Pentafluoro-2'-methoxy-5'-methyl-1,1'-biphenylHCID 5732780393%

Reaction Steps

Compound 5 (11.3 g, 45.54 mmol, 1 equiv) and iodopentafluorobenzene (10.6 g, 36.2 mmol, 1 equiv) were dissolved in toluene (200 mL) and 1.0M potassium carbonate solution (200 mL). Tetrabutylammonium bromide (1.6 g, 5 mmol, 0.11 equiv) was added and the solution sparged with nitrogen for 10 minutes. Tetrakis(triphenylphosphine)palladium(0) (2.63 g, 2.28 mmol, 0.05 equiv) was added and the reaction was refluxed for one day. The reaction was cooled to room temperature, then the layers were separated. The aqueous phase was back extracted with ethyl acetate (2×200 mL). Combined organic phases were combined, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified over silica gel (200 g), eluting with heptanes to give 2,3,4,5,6-pentafluoro-2′-methoxy-5′-methyl-1,1′-biphenyl (6) (9.7 g, 74% yield) as a pale-yellow oil. This material contained a small amount of unreacted iodopentafluorobenzene which was identified by 19F NMR. The material was used subsequently.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952114B2
Source datasetuspto-grants-2015_02
ORD IDord-e95ef93340a349c391c502c27ec4471d
Source noteuspto-grants-2015_02