HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl p-methylbenzenesulfonate → 1-(1-Ethyl-piperidin-4-yl)-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Piperidin-4-yl)-1H-indole | HCID 14090755 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(1-Ethyl-piperidin-4-yl)-indole | HCID 22907250 | — |
Reaction Steps
To a solution of 1-piperidin-4-yl-1H-indole (0.6 g, 3 mmol) in 5 mL of dry ethanol was added anhydrous potassium carbonate (680 mg, 4.9 mmol). After stirring for 15 minutes at ambient temperature, ethyl p-toluenesulfonate (0.48 mL,4.5 mmol) was added. The reaction was heated under reflux for 24 hours with stirring, quenched with water, extracted with methylene chloride (2×), dried and evaporated to give a residue. The residue was chromatographed on silica gel with toluene/acetone (50:50) to yield 360 mg straw colored material (53% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545636 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-b6a424f42d094085a3a902a435d7b003 |
| Source note | uspto-grants-1996_08 |