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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222468Generated: October 30, 2026

Methyl iodide → 5-fluoro-6-iodo-1-methyl-1H-indole

https://huagongshe.com/reaction/222468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-fluoro-6-iodo-1H-indoleHCID 22612772—
SolventDimethylformamideHCID 6228—
Product5-fluoro-6-iodo-1-methyl-1H-indoleHCID 6852429096.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-iodo-5-fluoro-1H-indole (0.495 g, 1.890 mmol) in dry DMF (7.0 mL) was added sodium hydride (55% suspension in oil) (0.124 g, 2.840 mmol) at 0° C. The mixture was stirred at 0° C. for 30 min, and then iodomethane (0.15 mL, 2.47 mmol) was added. The mixture was stirred for 1 hour at room temperature, and then quenched with ice and extracted with EtOAc (50 mL). The organic layer was washed with water, brine, dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography (EtOAc-hexane, 1:9) to afford 5-fluoro-6-iodo-1-methyl-1H-indole as a colorless solid (0.50 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207216B2
Source datasetuspto-grants-2012_06
ORD IDord-a508b61691fa4a808cabed1c880ca87c
Source noteuspto-grants-2012_06