2-Naphthol


2-Naphthol, or β-naphthol, is a fluorescent colorless crystalline solid with the formula C10H7OH. It is an isomer of 1-naphthol, differing by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, but more reactive. Both isomers are soluble in simple alcohols, ethers, and chloroform. 2-Naphthol is a widely used intermediate for the production of dyes and other compounds.

Production

Traditionally, 2-naphthol is produced by a two-step process that begins with the sulfonation of naphthalene in sulfuric acid:
The sulfonic acid group is then cleaved in molten sodium hydroxide:
Neutralization of the product with acid gives 2-naphthol.
2-Naphthol can also be produced by a method analogous to the cumene process.

2-Naphthol-derived dyes

The Sudan dyes are popular dyes noted for being soluble in organic solvents. Several of the Sudan dyes are derived from 2-naphthol by coupling with diazonium salts. Sudan dyes I -IV and Sudan Red G consist of arylazo-substituted naphthols.

Reactions

2-Naphthol reacts to form BINOL, a C2-symmetric ligand popularized for use in asymmetric catalysis.
2-Naphthol converts to 2-naphthalenethiol via reaction with dimethylthiocarbamoyl chloride via the Newman-Kwart rearrangement.

Safety

Naphthols are used as biomarkers for livestock and humans exposed to polycyclic aromatic hydrocarbons.