HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537026Generated: October 25, 2026
Iodine → 2-Fluoro-3-iodo-5-methylpyridine
https://huagongshe.com/reaction/537026
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2-Fluoro-5-methylpyridine | HCID 2774635 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-3-iodo-5-methylpyridine | HCID 10243220 | 499.3% |
Reaction Steps
A solution of 2M LDA in THF (371 mL, 742 mmol) was added to THF (1400 mL) at −78° C. under an atmosphere of nitrogen. To this stirred, cooled solution was added 2-fluoro-5-methylpyridine (75.0 g, 67.6 mmol) in THF (280 mL) dropwise. The reaction mixture was allowed to stir at −78° C. for 2 h and then a solution of iodine (171.5 g, 67.6 mmol) in THF (560 mL) was added dropwise. The reaction mixture was allowed to stir at −78 for 2 h and then diluted with water (875 mL). The mixture was allowed to warm to rt and was then extracted with EtOAc. The organic solutions were combined, washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to give 2-fluoro-3-iodo-5-methylpyridine (80 g, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08859768B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-16a6e59ce02b4fb3b5c3aec2a9000e59 |
|---|
| Source note | uspto-grants-2014_10 |
|---|