Aminonaphthalenesulfonic acids

Aminonaphthalenesulfonic acids are compounds with the composition C10H6(NH2)(SO3H), being derived from naphthalene (C10H8) substituted by an amino and sulfonic acid groups. These compounds are colorless solids. They are useful precursors to dyes.[1]

1-Aminonaphthalenesulfonic acids
IsomerCAS Registry NumberAlternative namesPreparative route
1-Aminonaphthalene-4-sulfonic acid 84-86-6Piria’s acid, naphthionic acidsulfonation of 1-aminonaphthalene
1-Aminonaphthalene-5-sulfonic acid84-89-9Laurent’s acid, L acid, Purpurin acidreduction of 1-nitronaphthalene-5-sulfonic acid
1-Aminonaphthalene-6-sulfonic acid119-79-91,6-Cleve’s acidsulfonation of 1-aminonaphthalene
1-Aminonaphthalene-7-sulfonic acid119-28-81,7-Cleve’s acidreduction of 1-nitroonaphthalene-8-sulfonic acid

Notes: Peri-acid dehydrates to the sultam. Via the Bucherer reaction, heating periacid with anilinium salts gives the N-phenyl derivative, precursor to Acid Blue 113.

2-Aminonaphthalenesulfonic acids
IsomerCAS Registry NumberAlternative namesPreparative route
2-Aminonaphthalene-1-sulfonic acid81-16-3Tobias acid Bucherer reaction of 2-hydroxynaphthalene-1-sulfonic acid with ammonium salts
2-Aminonaphthalene-5-sulfonic acid81-05-0Dahl’s acid, Dressel acid, D acidDesulfonation of 2-aminonaphthalene-1,5-disulfonic acid
2-Aminonaphthalene-6-sulfonic acid93-00-5 Bronner acidBucherer amination of 2-hydroxynaphthalene-6-sulfonic acid
2-Aminonaphthalene-7-sulfonic acid494-44-0 Amido F acidBucherer amination of 2-hydroxynaphthalene-7-sulfonic acid
2-Aminonaphthalene-8-sulfonic acid86-60-2Badische acidBucherer amination of 2-hydroxynaphthalene-8-sulfonic acid

References

  1. ↑ Gerald Booth "Naphthalene Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a17_009.
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