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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113128Generated: October 30, 2026

1-(Quinolin-4-yl)ethan-1-one → 1-(1-Methyl-1H-indol-4-yl)ethanone

https://huagongshe.com/reaction/2113128

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Quinolin-4-yl)ethan-1-oneHCID 12340190—
Reactant1-(1-Methyl-1H-indol-4-yl)-ethanolHCID 22391398—
CatalystManganese oxideHCID 160959—
SolventDichloromethaneHCID 6344—
Product1-(1-Methyl-1H-indol-4-yl)ethanoneHCID 14987288—

Reaction Steps

The title compound was prepared by the same procedure for 1-quinolin-4-yl-ethanone from 1-(1-Methyl-1H-indol-4-yl)-ethanol (3.0 g, 17 mmol), manganese oxide (8.69 g, 100 mmol, Aldrich) and dichloromethane (50 mL). The crude title compound was obtained in form as yellow oil in 98% yield (2.9 g, 16.7 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524873B2
Source datasetuspto-grants-2009_04
ORD IDord-f04b77a2bfc044c4a02d962e6b6de6fc
Source noteuspto-grants-2009_04