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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-aminonaphthalene-1-sulfonic acid | HCID 3091126 | — |
| Reactant | HCID 131726475 | HCID 131726475 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Product | HCID 178507492 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07297199B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-b4cb61b2dbef4e938af1e8a6c5c34b73 |
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| Source note | uspto-grants-2007_11 |
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