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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247551Generated: November 2, 2026

Indole → Ketone, indol-3-yl p-methoxyphenyl (6CI,8CI)

https://huagongshe.com/reaction/247551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantHCID 178418373HCID 178418373—
SolventDiethyl EtherHCID 3283—
ProductKetone, indol-3-yl p-methoxyphenyl (6CI,8CI)HCID 211017—

Reaction Steps

30 ml of ether solution containing 4.0 g of indole were added to 10 ml of ether solution containing 5.0 g of methylmagnesium iodide. And then 30 ml of ether solution containing 5.7 g of anisoyl chloride were added dropwise to the solution. The reaction mixture was allowed to stand for several hours and further refluxed for 3 hours. After cooling, the reaction mixture was washed with aqueous solution of sodium hydrogencarbonate. The obtained organic layer was evaporated to dryness under reduced pressure. After purification by chromatography on silica gel and recrystallization from ethanol, 3-(p-methoxybenzoyl)indole (compound 1) was obtained in the form of white crystals. (Yield: 42%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04708961
Source datasetuspto-grants-1987_11
ORD IDord-654df088391c4892a801d584e25a06a9
Source noteuspto-grants-1987_11