HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288650Generated: October 27, 2026
Methyl iodide → Methyl alpha,1-dimethyl-1H-indole-3-acetate
https://huagongshe.com/reaction/1288650
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Methyl 2-(1-methyl-1H-indol-3-yl)acetate | HCID 11106438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl alpha,1-dimethyl-1H-indole-3-acetate | HCID 11117483 | — |
Reaction Steps
To a solution of lithium diisopropyl amide, LDA, (5.5 millimole) in 10 mL of dry tetrahydrofuran at -78° C. was added dropwise a solution of methyl 2-(1-methyl-3-indolyl)acetate (1.02 g) in 3 mL of dry tetrahydrofuran. This mixture was stirred for one hour, then 1.42 g of methyl iodide was added and the mixture was warmed to room temperature and stirred for an additional 30 minutes. The mixture was poured into a solution of aqueous saturated ammonium chloride and then extracted with diethyl ether. The ether extract was dried over magnesium sulfate and concentrated to an oil by evaporation. The residue was subjected to silica gel chromatography using a developing solution of hexanes/ethyl acetate (6:1 by volume) to give 1.04 g of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747236 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-3e291ae7368a4eec8cdb440f682a0af6 |
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| Source note | uspto-grants-1998_05 |
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