HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-[2-(ethoxycarbonyl)ethyl]-N-(3-pyridyl)indole → 3-(2-formylethyl)-N-(3-pyridyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-[2-(ethoxycarbonyl)ethyl]-N-(3-pyridyl)indole | HCID 20270182 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-formylethyl)-N-(3-pyridyl)indole | HCID 13490354 | — |
Reaction Steps
A solution of 2.7 g of 3-[2-(ethoxycarbonyl)ethyl]-N-(3-pyridyl)indole in 50 ml of dry methylene chloride under nitrogen is cooled to -75° and 10.6 ml of 1.75M diisobutylaluminum hydride in toluene is added dropwise. The reaction is stirred for 8 minutes and quenched with 10 ml of water at -75°. Cooling is stopped and the layers are separated. The organic phase is washed with water, dried over potassium carbonate and evaporated to a solid which is recrystallized from ether-hexane to yield 3-(2-formylethyl)-N-(3-pyridyl)indole, m.p. 44°-45°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536505 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-7625907fc7ca40df970c49a316217051 |
| Source note | uspto-grants-1985_08 |