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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987444Generated: October 30, 2026

Bromobenzene → HCID 21891628, compound

https://huagongshe.com/reaction/987444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantPotassium HydroxideHCID 14797—
ReactantVGRVYVYBENLQJG-UHFFFAOYSA-NHCID 4715372—
CatalystCopper oxideHCID 14829—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 21891628HCID 21891628—

Reaction Steps

Methyl 4,5,6-trimethoxyindole-2-carboxylate (533 mg), bromobenzene (0.22 mL), copper oxide (64 mg) and potassium hydroxide (336 mg) were suspended in dry DMF (10 mL), and the suspension was refluxed and stirred for 6 hours under an argon atmosphere. After cooling, the reaction mixture was dissolved in water (100 mL) and filtered through celite. The filtrate was extracted with ethyl acetate, and the extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was dissolved in methanol (20 mL) and chloroform (20 mL), and water-soluble carbodiimide hydrochloride (192 mg) and N,N-dimethylaminopyridine (small amount) were added to the solution. The mixture was stirred overnight at room temperature. After concentrating the reaction mixture under reduced pressure, water was added to the residue to conduct extraction with ethyl acetate. The resultant organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by preparative TLC on silica gel (ethyl acetate:hexane=1:3) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632810B2
Source datasetuspto-grants-2003_10
ORD IDord-8e6453c4e353458ea0a2805176521948
Source noteuspto-grants-2003_10