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1 | P a g e
Preparation of Naphthalene derivatives
1. Naphthols
a) Preparation of Naphthols:
There are 2 isomeric naphthols
i) Fusion of naphthalene-1-sulphonic acid with NaOH gives 1-naphthol or -naphthol
ii) Similarly fusion of naphthalene-2-sulphonic acid with NaOH gives 2-naphthol or
-naphthol.
iii) Pure 1-naphthol is prepared by heating 1-naphthyl amine with dil.H2SO4 at 300oC
under pressure.
2 | P a g e
Reactions of naphthols
i) Electrophilic substitution reactions:
They undergo halogenation, nitration, sulphonation, etc.
ii) They reduce ammonical silver nitrate (Tollen’s reagent)
iii) Reduction : They are reduced by sodium and isoamyl alcohol to yield
tetrahydronaphthols.
iv) Reaction with nitrous acid: They react with nitrous acid to form monoximes like
resorcinol or phloroglucinol.
Similarly -naphthol forms -Naphthaquinone-1-oxime
3 | P a g e
v) Oxidation: They are oxidised by alkaline permanganate to phthalonic acid.
-Naphthol is oxidised to -naphthaquinone by chromic acid.
Prepared by
Dr. A. Syed Mohamed
HoD and Senior Assistant Professor, Research Dept. of Chemistry
Sadakathullah Appa College (Autonomous)
Tirunelveli, Tamilnadu, India. asm2032@gmail.com
The author ackowledges Prof. H. Kassali Rahmathullah, Dr. T. Syed Ismail, Dr. M.
Kamalutheen, Former Professor, Dept. of Chemistry, Sadakathullah Appa College for their
valuable contribution.

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Polynuclear hydrocarbons Module3

  • 1. 1 | P a g e Preparation of Naphthalene derivatives 1. Naphthols a) Preparation of Naphthols: There are 2 isomeric naphthols i) Fusion of naphthalene-1-sulphonic acid with NaOH gives 1-naphthol or -naphthol ii) Similarly fusion of naphthalene-2-sulphonic acid with NaOH gives 2-naphthol or -naphthol. iii) Pure 1-naphthol is prepared by heating 1-naphthyl amine with dil.H2SO4 at 300oC under pressure.
  • 2. 2 | P a g e Reactions of naphthols i) Electrophilic substitution reactions: They undergo halogenation, nitration, sulphonation, etc. ii) They reduce ammonical silver nitrate (Tollen’s reagent) iii) Reduction : They are reduced by sodium and isoamyl alcohol to yield tetrahydronaphthols. iv) Reaction with nitrous acid: They react with nitrous acid to form monoximes like resorcinol or phloroglucinol. Similarly -naphthol forms -Naphthaquinone-1-oxime
  • 3. 3 | P a g e v) Oxidation: They are oxidised by alkaline permanganate to phthalonic acid. -Naphthol is oxidised to -naphthaquinone by chromic acid. Prepared by Dr. A. Syed Mohamed HoD and Senior Assistant Professor, Research Dept. of Chemistry Sadakathullah Appa College (Autonomous) Tirunelveli, Tamilnadu, India. asm2032@gmail.com The author ackowledges Prof. H. Kassali Rahmathullah, Dr. T. Syed Ismail, Dr. M. Kamalutheen, Former Professor, Dept. of Chemistry, Sadakathullah Appa College for their valuable contribution.