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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869759Generated: October 27, 2026

Benzonitrile, 4-bromo- → 4-(Pentafluoroethyl)benzonitrile

https://huagongshe.com/reaction/1869759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrile, 4-bromo-HCID 12162—
ReactantSodium pentafluoropropionateHCID 2733305—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-(Pentafluoroethyl)benzonitrileHCID 14774185—

Reaction Steps

4-Bromobenzonitrile (10 g, 54.9 mmol), sodium pentafluoropropionate (26.5 g, 0.143 mol) and copper (I) iodide (27.1 g, 0.142 mol) were heated to 150° C. in dry DMF (130 ml) for 4 h. The reaction mixture was diluted with water and Et2O and kieselgur filter aid was added. This bi-phasic mixture was stirred for 5 min, filtered and separated. The aqueous phase was extracted with Et2O. The combined organic phases were washed with water and aq. NH3, then dried over MgSO4, filtered and concentrated under reduced pressure to give the crude product as a brown oil. This was purified by flash chromatography (silica gel, 20-30% DCM in iso-hexanes) to give the title compound, 7.5 g (62%). 1H NMR (500 MHz, CDCl3): δ 7.75 (2H, d, J 8.3), 7.83 (2H, d, J 8.6), 19F NMR (470 MHz, CDCl3): δ −84.5, −116.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638629B2
Source datasetuspto-grants-2009_12
ORD IDord-732ec2b3d66240d59260d6edf1165d25
Source noteuspto-grants-2009_12