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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425579Generated: November 3, 2026

4-methoxy-N-(4-nitrophenyl)aniline → HCID 10243439, compound

https://huagongshe.com/reaction/1425579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-methoxy-N-(4-nitrophenyl)anilineHCID 2748023—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetic AcidHCID 176—
ProductHCID 10243439HCID 1024343964%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 4-methoxy-N-(4-nitrophenyl)aniline (785 mg, 3.2 mmol) in 5 mL of AcOH was added Pd(OAc)2 (1.43 g, 6.4 mmol). The mixture was heated at 100° C. for 15 h under air atmosphere and cooled to rt and concentrated under reduced pressure. The residue was taken up in EtOAc (100 mL) and washed with NaHCO3 (2×100 mL) and water (100 mL). After solvent removal, the crude was purified with chromatography (hexane/EtOAc) to afford 3-methoxy-6-nitro-9H-carbazole as a orange solid (495 mg, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08932557B2
Source datasetuspto-grants-2015_01
ORD IDord-f5757a4643744252ba87507373ee78db
Source noteuspto-grants-2015_01