HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775849Generated: October 31, 2026
Sodium Iodide → 5-Bromo-2-iodo-4-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/1775849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 5-Bromo-2-chloro-4-(trifluoromethyl)pyridine | HCID 37859478 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Bromo-2-iodo-4-(trifluoromethyl)pyridine | HCID 86689700 | 40% |
Reaction Steps
Prepared using General Procedure 17: To a stirred a solution of 5-bromo-2-chloro-4-(trifluoromethyl)pyridine (150 mg, 0.576 mmol) in acetonitrile (2 mL) was added sodium iodide (518 mg, 3.45 mmol). The reaction mixture was heated to 40° C. and acetyl chloride (26.0 mg, 0.345 mmol) was added. The reaction mixture was stirred at 40° C. for 90 min. Once cooled, the reaction was quenched with NaHCO3 (5 mL) and extracted with EA (3×5 mL). The combined organics were washed with brine (10 mL), dried over MgSO4 and concentrated to give 80.0 mg (40%) of 5-bromo-2-iodo-4-(trifluoromethyl)pyridine as a white crystalline solid which was used in the subsequent step without purification. LCMS-ESI (m/z) calculated for C6H2BrF3IN, 351.9. found 352.5 [M+H]+, tR=3.91 min. (Method 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260427B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-b9e55e87c1b74a90bc946769fab6f776 |
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| Source note | uspto-grants-2016_02 |
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