Synthesis of Fluorescein

Synthesis of Fluorescein from Resorcinol and phthalic Acid

Synthesis of Fluorescein from Resorcinol and phthalic Acid

This fluorescent dye was first synthesized by Adolf von Baeyer in the 19th century. This is an acid catalysed reaction between resorcinol and phthalic anhydride.

Synthesis of Fluorescein from Resorcinol and phthalic Acid

Mechanism of Synthesis of Fluorescein from Resorcinol and Phthalic Acid

The following mechanism of the fluorescein synthesis was performed by von Baeyer involves mainly in two steps:
1. Friedel-Crafts Acylation and
2. Formation of Fluorescein.
Hydroxyl group of resorcinol acts as a nucleophile which attacks the carbonyl carbon of phthalic anhydride and forms an intermediate compound through electrophilic aromatic substitution. The reaction further proceeds through electrophilic substitutions that ultimately forms fluorescein. Presence of sulfuric acid in this synthesis increases the electrophilicity of phthalic anhydride.

Mechanism of Synthesis of Fluorescein from Resorcinol and phthalic Acid

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B.Sc. Chemistry
2nd and 4th Semester


CUET (UG) Exam 2025


ORGANIC CHEMISTRY
Special Batch for NEET


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Online Class: 26 March 2025