HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372691Generated: October 31, 2026
Water → Methyl 1-(1-methylethyl)-1H-indole-3-carboxylate
https://huagongshe.com/reaction/1372691
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl indole-3-carboxylate | HCID 589098 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-(1-methylethyl)-1H-indole-3-carboxylate | HCID 10443342 | 78% |
Reaction Steps
In DMF (8.0 ml) was suspended sodium hydride (60% in oil, 275.2 mg, 6.881 mmol). To the resulting suspension was added methyl indole-3-carboxylate (401.8 mg, 2.294 mmol) at 0° C. under stirring. After stirring for further 45 minutes at the same temperature, isopropyl iodide (0.34 ml, 3.440 mmol) was added to the reaction mixture. Stirring was then conducted for 1.5 hours at 0° C. and for 7 hours at room temperature. Water was added to the reaction mixture to terminate the reaction, followed by extraction with ethyl acetate. The extract was washed successively with 1N HCl and saturated saline, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from hexane-ethyl acetate (3:1, v/v) eluate fractions, methyl 1-isopropylindole-3-carboxylate (387.6 mg, 78%) was obtained as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-6f51e8baaa8a47e393f5c62643d31f7e |
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| Source note | uspto-grants-2007_01 |
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