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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579669Generated: October 26, 2026

5-Nitro-4-amino-1-naphthol → 5-Nitronaphthalene-1,4-dione

https://huagongshe.com/reaction/1579669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitro-4-amino-1-naphtholHCID 21569005—
ReactantHCID 178516261HCID 178516261—
ReactantHCID 178516262HCID 178516262—
CatalystFerrous cationHCID 27284—
Product5-Nitronaphthalene-1,4-dioneHCID 12336402—

Reaction Steps

5-Nitro-1,4-naphthoquinone is prepared by reducing 8-nitro-1,4-naphthoquinone-1-oxime and/or 5-nitro-1,4-naphthoquinone-1-oxime in an aqueous and/or organic reaction medium in the presence of iron (II) ions and a hydrogen halide at a temperature in the range of from -20° to 100°C, and thereafter oxidizing the 8- and and/or 5-nitro-4-amino-1-naphthol formed, or the corresponding salt, optionally without intermediate isolation, at a temperature in the range of from -10° to 100°C to form the desired 5-nitro-1,4-naphthoquinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931255
Source datasetuspto-grants-1976_01
ORD IDord-0086968c91504490ba5b4f7d4f16714a
Source noteuspto-grants-1976_01