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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Fluoro-5-iodobenzonitrile | HCID 2778928 | — |
| Reactant | 3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)pyrrolidine | HCID 58218880 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-[3-(3,5-Dichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]2-fluorobenzonitrile | HCID 58218889 | 63.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980937B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9031a5e1cfac4ac4aba8169a8644e41b |
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| Source note | uspto-grants-2015_03 |
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