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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401487Generated: October 29, 2026

6-Chloro-2-iodo-3-(trifluoromethyl)pyridine → (6-Chloro-3-(trifluoromethyl)pyridin-2-yl)(2-fluoropyridin-3-yl)methanone

https://huagongshe.com/reaction/401487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-2-iodo-3-(trifluoromethyl)pyridineHCID 11220536—
Reactant2-Fluoro-N-methoxy-N-methylnicotinamideHCID 53417067—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product(6-Chloro-3-(trifluoromethyl)pyridin-2-yl)(2-fluoropyridin-3-yl)methanoneHCID 5769054461%

Reaction Steps

To a solution of 6-chloro-2-iodo-3-(trifluoromethyl)pyridine (described in the literature: Eur. J. Org. Chem. 2004, 3793) (1.9 g, 6.180 mmol) in tetrahydrofuran (20 mL), cooled to −78° C., was added isopropyl magnesium chloride 2M in tetrahydrofuran (3.152 mL of 2 M, 6.304 mmol). The reaction mixture was stirred for 15 minutes. A solution of 2-fluoro-N-methoxy-N-methylnicotinamide (1.252 g, 6.798 mmol) in tetrahydrofuran (4 mL) was added and the reaction mixture was stirred at −78° C. for 1 hour. The reaction mixture was partitioned between a saturated solution of ammonium chloride and ethyl acetate. The organic extract was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as a pale yellow oil (1.14 g, 61% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741931B2
Source datasetuspto-grants-2014_06
ORD IDord-e45b1099a5564c2bb0682060eac90451
Source noteuspto-grants-2014_06