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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533105Generated: October 26, 2026

Indole → 2-(1H-indol-3-yl)quinoline

https://huagongshe.com/reaction/1533105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantBenzoyl chlorideHCID 7412—
ReactantQuinoline 1-oxideHCID 15366—
SolventDichloromethaneHCID 6344—
Product2-(1H-indol-3-yl)quinolineHCID 124066226%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of quinoline-N-oxide (0.5 mmol) in 2 mL DCM at 0° C. in a 3 mL plastic tube fitted with a frit was added 58 uL of benzoyl chloride (0.5 mmol). The reaction mixture was stirred for 15 min at 0° C. and then indole (0.5 mmol) was added. The reaction was warmed to 20° C. and stirred for 4 h. The solid precipitate was filtered and washed with DCM (3×2 mL) to give solid 2-(3-indolyl)quinoline (6-100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207679B1
Source datasetuspto-grants-2001_03
ORD IDord-628d7da26e5d4ea89202445dcbb6c36b
Source noteuspto-grants-2001_03