HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564975Generated: October 30, 2026
Methyl iodide → Methyl 1-(1-methylethyl)-1H-indole-5-carboxylate
https://huagongshe.com/reaction/564975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 178053-59-3 | HCID 21194436 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-(1-methylethyl)-1H-indole-5-carboxylate | HCID 15550263 | — |
Reaction Steps
A mixture of 2.20 g (8.97 mmol) of isopropyl 1-isopropyl-5-indolecarboxylate, 100 ml of 2N sodium hydroxide solution and 100 ml of ethanol was refluxed for an hour. The solvent was then distilled off under reduced pressure. Thereafter water was added to the residue and the resulting mixture was acidified with conc. hydrochloric acid. The precipitated solid was filtered and dried under reduced pressure to give 2.00 g of crude 1-isopropyl-5-indole-carboxylic acid. The reaction was carried out in a manner similar to Reference Example 4 using 2.00 g of the crude 1-isopropyl-5-indolecarboxylic acid, 0.44 g (11.1 mmol) of 60% sodium hydride, 2.87 g (20.2 mmol) of methyl iodide and 50 ml of dimethyl-formamide. Thus, 1.64 g (84.2%; yield based on isopropyl 1-isopropyl-5-indolecarboxylic acid) was obtained.
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-938dcd2aeffe4867beed5a237aa35cde |
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| Source note | uspto-grants-2001_01 |
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