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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565050Generated: October 30, 2026

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

https://huagongshe.com/reaction/565050

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 numberUS06169107A
Source datasetuspto-grants-2001_01
ORD IDord-ea34c92f357e4de4896c01461489c2e5
Source noteuspto-grants-2001_01