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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816862Generated: November 2, 2026

1,2-Dichlorobenzene → HCID 57879965, compound

https://huagongshe.com/reaction/1816862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant2-PhenylindoleHCID 13698—
CatalystCopperHCID 23978—
SolventTolueneHCID 1140—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 57879965HCID 5787996550.1%

Reaction Steps

50.0 g (177 mmole) of 4-bromoiodobenzene, 28.5 g (177 mmole) of 2-phenylindole, 30.5 g (221 mmole) of potassium carbonate, 18.7 g of copper powder, and 150 ml of o-dichlorobenzene were put in a 500 ml three-necked flask, and refluxed with stirring for 25 hours under nitrogen flow. Toluene was added to the reaction mixture heated under stirring at 60° C., and insoluble matter was filtered off. The filtrate was vacuum dried. Hexane was added to the residue and deposited crystal was filtered off. The filtrate was condensed, and refined by silica gel column chromatography (eluent:hexane/ethyl acetate: 50/1), recrystallized with a mixed solvent of hexane/ethyl acetate to give 25.7 g of a white crystal of 1-(4-bromophenyl)-2-phenylindole (yield: 50.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07597955B2
Source datasetuspto-grants-2009_10
ORD IDord-e0963ecf552c407d8e4654c0f33da8c9
Source noteuspto-grants-2009_10