HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481777Generated: November 1, 2026
Iodine → Tert-butyl 5-chloro-2,4-difluoro-6-iodonicotinate
https://huagongshe.com/reaction/1481777
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Tert-butyl 5-chloro-2,4-difluoronicotinate | HCID 71281897 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 5-chloro-2,4-difluoro-6-iodonicotinate | HCID 89421790 | 67% |
Reaction Steps
Into a solution of TMPMgCl LiCl (1.0 M×2.4 mL, 2.4 mmol) in THF at −45° C. was added dropwise a solution of tert-butyl 5-chloro-2,4-difluoronicotinate (0.4 g, 1.6 mmol) in THF (3.0 mL). The mixture was stirred for 20 min then iodine (0.61 g, 2.4 mmol) was added. After 15 min at −45° C., the temperature was allowed to warm to 0° C. The reaction was quenched with saturated NH4Cl and extracted with ethyl acetate. The organic layers were combined, dried over sodium sulfate and evaporated. The residue was purified by silica chromatography (0-5% ethyl acetate in hexanes) to give tert-butyl 5-chloro-2,4-difluoro-6-iodonicotinate (0.4 g, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409905B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-e72e5152d7ec4c9fb8e8b0eca50611b4 |
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| Source note | uspto-grants-2016_08 |
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