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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874778Generated: October 26, 2026

2-Fluoro-5-iodobenzonitrile → 5-[3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]2-fluorobenzonitrile

https://huagongshe.com/reaction/874778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-iodobenzonitrileHCID 2778928—
Reactant3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)pyrrolidineHCID 58218880—
SolventTolueneHCID 1140—
Product5-[3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]2-fluorobenzonitrileHCID 5821888963.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-(3,5-dichlorophenyl)-3-(trifluoromethyl)pyrrolidine (0.6 g) and 2-fluoro-5-iodobenzonitrile (0.57 g) was dissolved in toluene, which was then degassed 3 times. To the solution in toluene was added sodium tert-butoxide (0.20 g), Tris(dibenzylidene acetone)dipalladium chloroform complex (0.04 g) and Xantphos (0.07 g) under argon atmosphere, and the mixture was stirred at 80° C. for two hours. The mixture was cooled to room temperature and then diluted with ethyl acetate, which was then washed with water and dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the solvent was distilled away under the reduced pressure, and the residue was then purified by silica gel chromatography to yield 5-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]-2-fluorobenzonitrile (0.54 g). m.p. 184-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980937B2
Source datasetuspto-grants-2015_03
ORD IDord-9031a5e1cfac4ac4aba8169a8644e41b
Source noteuspto-grants-2015_03