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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485339Generated: October 26, 2026

3-[2-(ethoxycarbonyl)ethyl]-N-(3-pyridyl)indole → 3-(2-formylethyl)-N-(3-pyridyl)indole

https://huagongshe.com/reaction/485339

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[2-(ethoxycarbonyl)ethyl]-N-(3-pyridyl)indoleHCID 20270182—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product3-(2-formylethyl)-N-(3-pyridyl)indoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536505
Source datasetuspto-grants-1985_08
ORD IDord-7625907fc7ca40df970c49a316217051
Source noteuspto-grants-1985_08