HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 19795531, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-methoxy-3-methyl-1H-indole | HCID 326653 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 19795531 | HCID 19795531 | 72.2% |
Reaction Steps
4.6 g of 3-methyl-6-methoxyindole [Chem. ber. 98, 1727 (1965)] are presented in 29 ml of dimethyl sulfoxide. 6.6 ml of 10n aqueous KOH are then added, and 3.25 g of ethyl bromide are added dropwise at 20° C. in the course of 30'. 1 hour later the reaction mixture is poured onto water and extracted with toluene. Chromatography over silica gel (hexane/ether 5:1) gives 3.9 g of 1-ethyl-3-methyl-6-methoxyindol in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05071986 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-d876e6fbcd3f49899a1f0e724f9ee842 |
| Source note | uspto-grants-1991_12 |