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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593345Generated: October 30, 2026

3-aminonaphthalene-1-sulfonic acid → HCID 178507492, compound

https://huagongshe.com/reaction/1593345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-aminonaphthalene-1-sulfonic acidHCID 3091126—
ReactantHCID 131726475HCID 131726475—
ReactantHCID 178418936HCID 178418936—
ProductHCID 178507492HCID 178507492—

Reaction Steps

Diazotized 4-nitro-4′-aminostilbene-2,2-disulfonic acid and 3-aminonaphthalene-1-sulfonic acid were subjected to coupling. The resultant was turned into a triazole, and a nitro group of the triazole was reduced to an amino group by means of a conventionally known method to produce aminostilbene-triazole. Aminostilbene-triazole was dissolved into water, and sodium nitrite and hydrochloric acid were added dropwise to the solution to perform diazotization. The resultant was added dropwise to an aqueous solution of a compound represented by Compound (1) below, and the whole was subjected to coupling, followed by dialysis with sodium chloride. The compound was diazotized with an aqueous solution of sodium nitrite, and was turned into a triazole by adding an aqueous solution of 6-aminonaphthalene-2-sulfonic acid. The triazole was dialyzed with sodium chloride to prepare a coloring material (sodium salt) represented by the general formula (I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297199B2
Source datasetuspto-grants-2007_11
ORD IDord-b4cb61b2dbef4e938af1e8a6c5c34b73
Source noteuspto-grants-2007_11