HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41062Generated: October 23, 2026
Potassium Carbonate → 5-(2-methoxyethoxy)-1H-indole
https://huagongshe.com/en/reaction/41062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Hydroxyindole | HCID 16054 | — |
| Reactant | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| Reactant | Acetone 2-methoxyethyl iodide | HCID 86634331 | — |
| Solvent | Toluene acetone | HCID 20247278 | — |
| Product | 5-(2-methoxyethoxy)-1H-indole | HCID 10352537 | 86.2% |
Reaction Steps
To a solution of 5-hydroxy-indole (15.2 g, 114 mmol) in 250 ml of dry acetone 2-methoxyethyl iodide (15 ml, 141 mmol, 1.25 equiv) and anhydrous K2CO3 (46.7 g, 338 mmol, 3 equiv) are added and the mixture is refluxed. Additional amounts of 0.5 equiv of 2-methoxyethyl iodide and K2CO3 are added each day. After 6 days TLC (toluene-acetone, 9:1) indicates the absence of starting material. The solid is removed by filtration, and the solvent is evaporated. The residue is taken up in dichloromethane (800 ml) and the solution is washed with 2 M aqueous HCl, 10% aqueous NaHCO3, and water. The organic layer is dried and concentrated. Column chromatography (toluene-acetone, 9:1) provides 5-(2-methoxyethoxy)-1H-indole (18.8 g, 86%). M.p. 58-60° C. (from ethyl acetate-light petroleum).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08530493B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-a397b75c02ed433587cf9bf2dbd0b0f4 |
|---|
| Source note | uspto-grants-2013_09 |
|---|