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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067836Generated: November 2, 2026

Sodium hydride → Ethyl 4-chloro-6-(4-formylphenoxy)-1-methyl-2-indolecarboxylate

https://huagongshe.com/reaction/1067836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantEthyl 4-chloro-6-hydroxy-1-methyl-2-indolecarboxylateHCID 21194263—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-chloro-6-(4-formylphenoxy)-1-methyl-2-indolecarboxylateHCID 2119419164.6%

Reaction Steps

After 1.00 g (3.94 mmol) of ethyl 4-chloro-6-hydroxy-1-methyl-2-indolecarboxylate was added to a suspension of 0.16 g (3.94 mmol) of 60% sodium hydride and 30 ml of dimethylformamide, the suspension was stirred at room temperature until the mixture became an almost transparent solution. Then 0.54 g (4.34 mmol) of 4-fluoro-benzaldehyde was added to the solution at room temperature followed by stirring for 10 hours at 70° C. The reaction mixture was poured onto ice water. The resulting mixture was then extracted three times with ethyl acetate. The combined extracts were washed with water. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was isolated and purified by silica gel column chromatography to give 0.91 g (64.5%) of ethyl 4-chloro-6-(4-formylphenoxy)-1-methyl-2-indolecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248772B1
Source datasetuspto-grants-2001_06
ORD IDord-226ca4bd15da4d8e83fa50acab33c562
Source noteuspto-grants-2001_06