HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroacetate → (1H-Indol-6-yloxy)-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroacetate | HCID 7295 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Hydroxyindole | HCID 524508 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (1H-Indol-6-yloxy)-acetic acid methyl ester | HCID 18969559 | 63.3% |
Reaction Steps
6-Hydroxyindole (2.9 g), methyl chloroacetate (2.7 g), potassium carbonate (5.5 g) and potassium iodide (0.2 g) are added to acetone (100 ml), and the mixture is refluxed for 8 hours. The reaction mixture is cooled to room temperature, and the insoluble materials are removed by filtration. The filtrate is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent; chloroform) to give 6-methoxycarbonylmethoxyindole (2.83 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05817689 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-59f19f98a90542538f9d78d9b52ab590 |
| Source note | uspto-grants-1998_10 |