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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015433Generated: October 31, 2026

Sodium hydride → HCID 67300756, compound

https://huagongshe.com/reaction/1015433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantHCID 67300353HCID 67300353—
SolventDimethylformamideHCID 6228—
ProductHCID 67300756HCID 67300756—

Reaction Steps

A 500 mg portion of ethyl 2-ethyl-3-methyl-1H-indole-5-carboxylate was dissolved in 10 ml of N,N-dimethylformamide, and 113 mg of sodium hydride (55% dispersion in oil) was added under ice-cooling, followed by stirring at room temperature for 30 minutes. Then, 490 mg of 1-(bromomethyl)-4-fluorobenzene was added under ice-cooling, followed by stirring at room temperature for 2 hours. After evaporation of the solvent under a reduced pressure, the residue was diluted with ethyl acetate and washed with water and saturated brine. After drying the organic layer with anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:20 to 1:0) to obtain 587 mg of ethyl 2-ethyl-1-(4-fluorobenzyl)-3-methyl-1H-indole-5-carboxylate as a pale brown oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985764B2
Source datasetuspto-grants-2011_07
ORD IDord-f03bfc3af19740e8855c4edf4ca85509
Source noteuspto-grants-2011_07