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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Chloro-2-iodo-3-(trifluoromethyl)pyridine | HCID 11220536 | — |
| Reactant | 2-Fluoro-N-methoxy-N-methylnicotinamide | HCID 53417067 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Chloro-3-(trifluoromethyl)pyridin-2-yl)(2-fluoropyridin-3-yl)methanone | HCID 57690544 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741931B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-e45b1099a5564c2bb0682060eac90451 |
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| Source note | uspto-grants-2014_06 |
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