HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170849Generated: October 29, 2026
Sodium hydride → 1H-Indole-5-carboxylic acid, 1-(2-methoxyethyl)-, methyl ester
https://huagongshe.com/reaction/2170849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | methyl 1H-indole-5-carboxylate | HCID 2737635 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1H-Indole-5-carboxylic acid, 1-(2-methoxyethyl)-, methyl ester | HCID 67169484 | 50% |
Reaction Steps
To a stirred solution of methyl 1H-indole-5-carboxylate (200 mg, 1.14 mmol) and sodium hydride (60% in oil, 39 mg, 1.71 mmol) in N,N-dimethylformanide (3 mL) was added 1-bromo-2-methoxyethane (190 mg, 1.37 mmol) at room temperature. Then the mixture was stirred at 60° C. for 2 hours. The mixture was poured into water (20 mL) and extracted with ethyl acetate (20 mL). The organic layer was washed with water (20 mL) and dried over sodium sulfate. After removal of the solvent, the residue was purified by column chromatography on silica gel eluting with n-hexane/ethyl acetate (2:1) to give 132 mg (50%) of the title compound as colorless syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051296B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-6cb6d67f4d0b4e939f6ee6e390536e4f |
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| Source note | uspto-grants-2015_06 |
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