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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | Ethyl 4-chloro-6-hydroxy-1-methyl-2-indolecarboxylate | HCID 21194263 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-chloro-6-(4-formylphenoxy)-1-methyl-2-indolecarboxylate | HCID 21194191 | 64.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169107A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-ea34c92f357e4de4896c01461489c2e5 |
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| Source note | uspto-grants-2001_01 |
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