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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716428Generated: October 30, 2026

Sodium Iodide → 5-Bromo-2-iodo-4-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/716428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetyl chlorideHCID 6367—
Reactant5-Bromo-2-chloro-4-(trifluoromethyl)pyridineHCID 37859478—
SolventAcetonitrileHCID 6342—
Product5-Bromo-2-iodo-4-(trifluoromethyl)pyridineHCID 8668970040%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187522B2
Source datasetuspto-grants-2015_11
ORD IDord-242c81e4b88d4945bec6658886a8a7d3
Source noteuspto-grants-2015_11