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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61305Generated: October 25, 2026

Indole → 1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone

https://huagongshe.com/reaction/61305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
ReactantHCID 178418689HCID 178418689—
Product1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanoneHCID 4333928749%

Reaction Conditions

Temperature0 °C

Reaction Steps

Indole (11.7 g, 100 mmol) was dissolved in diethylether (100 ml) under nitrogen atmosphere and cooled to 0° C. 3M MeMgBr solution (35 ml, 105 mmol) was added dropwise and allowed to stir at room temperature for 2 hours. The reaction mixture was cooled at 0° C. and a solution of 2-methoxybenzoyl chloride 2 (18.46 g, 100 mmol) in diethyl ether (100 ml) was added dropwise with vigorous stirring. The reaction mixture was then allowed to stir at room temperature for 2 hours. A solution of ammonium chloride (300 ml) was added to the reaction mixture and the resulting mixture was stirred at room temperature overnight. The solid that was formed was collected by filtration, washed with water and hexane then dried in a dessicator over phosphorous pentoxide to give 13 g (49%) of 1-(1H-indol-3-yl)-2-(2-methoxyphenyl)ethanone 3 as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09441033B2
Source datasetuspto-grants-2016_09
ORD IDord-b5376fe189c74b34a9fb1889a1d962d7
Source noteuspto-grants-2016_09