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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25817Generated: October 25, 2026

Acetone → 6-Bromo-2,2,4-trimethyl-1,2-dihydroquinoline

https://huagongshe.com/reaction/25817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCatecholHCID 289—
ReactantIodineHCID 807—
Reactant4-BromoanilineHCID 7807—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Product6-Bromo-2,2,4-trimethyl-1,2-dihydroquinolineHCID 1072946427%

Reaction Steps

4-Bromoaniline (50 g, 0.290 mol), magnesium sulfate (250 g, 2 mol), iodine (2.5 g, 0.01 mol) and catechol (2.24 g, 0.020 mol) were combined in acetone (750 mL) in a sealed-tube reaction flask. The reaction vessel was placed in a pre-equilibrated oil bath set at 125° C. and stirred overnight. The reaction mixture was then cooled to room temperature, filtered over a pad of diatomaceous earth, and concentrated in vacuo. Chromatography on silica gel provided 6-bromo-2,2,4-trimethyl-1,2-dihydroquinoline as tan colored crystals (21 g, 27% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858627B2
Source datasetuspto-grants-2005_02
ORD IDord-bc6bae7813934b2eac71c44d75ed28f3
Source noteuspto-grants-2005_02