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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716694Generated: October 30, 2026

Ethanol → 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionaldehyde

https://huagongshe.com/reaction/1716694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionic acid ethyl esterHCID 59831728—
SolventDichloromethaneHCID 6344—
Product3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionaldehydeHCID 59831913—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. solution of 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionic acid ethyl ester CXVII (0.39 g, 1.2 mmol) in DCM (10 ml) was added DIBALH (1M in hexane, 4.0 ml, 4.0 mmol). After stirring for 90 minutes at −78° C., more DIBALH (1M in hexane, 1.2 ml, 1.2 mmol) was added. The resulting mixture was stirred for 2.25 hours, after which EtOH (2 ml) and a saturated solution of NaHCO3 (2 ml) were added. The mixture was then stirred at room temperature for 30 min, filtered, and the filter cake was washed with EtOAc. The filtrate was concentrated and washed with a saturated solution of NaHCO3, dried over Na2SO4, filtered, concentrated, and purified via flash chromatography (hexane/EtOAc) affording 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionaldehyde CXVIII as a colorless syrup (0.27 g, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803830B2
Source datasetuspto-grants-2010_09
ORD IDord-c057ca2fb8a242988488dd7b8b63fcd5
Source noteuspto-grants-2010_09