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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905536Generated: October 30, 2026

Quinoline → 2,7-bis(N-phenylacetylamino)dibenzodioxin

https://huagongshe.com/reaction/905536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
ReactantPotassium CarbonateHCID 11430—
ReactantIodobenzeneHCID 11575—
Reactant2,7-Bis(acetylamino)dibenzodioxinHCID 57892507—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,7-bis(N-phenylacetylamino)dibenzodioxinHCID 67389094—

Reaction Conditions

Temperature170 °C

Reaction Steps

A slurry prepared from 34.3 g (0.115 mole) of 2,7-bis(acetylamino)dibenzodioxin, 96.4 g (0.576 mole) of iodobenzene, 48.2 g (0.253 mole) of copper (I) iodide, 63.6 g (0.460 mole) of potassium carbonate, and 1500 ml of quinoline was heated with stirring at 170° C. for 48 hours. The reaction mixture was cooled to room temperature, 500 ml of methylene chloride and 500 ml of water were added, and a precipitate was separated by filtration. To the filtrate was added 500 ml of water and the organic layer was separated from the aqueous layer. The organic layer was concentrated and dried under reduced pressure to give 79.4 g of a crude product which was used without purification in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012606B2
Source datasetuspto-grants-2011_09
ORD IDord-9374108a7280443e8dba6ab2123f1ac4
Source noteuspto-grants-2011_09