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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404143Generated: November 2, 2026

Iodoethane → 6-bromo-1-ethyl-4-methoxy-1H-indole

https://huagongshe.com/reaction/1404143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-4-methoxy-1H-indoleHCID 24728034—
SolventDimethylformamideHCID 6228—
Product6-bromo-1-ethyl-4-methoxy-1H-indoleHCID 5830390970%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (96 mg, 4 mmol) was suspended in 7 mL DMF in a round bottom flask and cooled to 0° C. 6-bromo-4-methoxy-1H-indole (0.75 g, 3.3 mmol) was added dropwise as a solution in DMF (1 mL). Ethyl iodide (0.28 mL, 3.5 mmol) was added dropwise and the reaction mixture was stirred for 10 min. Volatiles were removed under reduced pressure and the residue partitioned between DCM and water. The aqueous layer was extracted with DCM and the combined organics layers were dried over MgSO4, filtered, and evaporated to give a red oil. The resulting residue was purified on silica gel column chromatography eluting with hexanes/ethyl acetate (0-10%) to afford pure 36-2 (584 mg, 70%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912220B2
Source datasetuspto-grants-2014_12
ORD IDord-46ae00ab12b14aad83e3e3d37620f1fb
Source noteuspto-grants-2014_12