Modified Methods for the Synthesis of Triazinyl Fluorescent Brightener Intermediates

The production of triazinyl fluorescent brightener intermediates in high yields is described. The method involves a simplified work-up for the preparation of 4-nitro-toluene-2-sulfonic acid and the use of diethylene glycol instead of water in the preparation of 4,4'-dinitrostilbene-2,2'-disulfonic acid.


Results and Discussion
In the common procedures for the separation of 2 after the sulfonation of 4-nitrotoluene (1) (Scheme 1), compound 2 is converted into the corresponding salt. Subsequently it is extracted from the reaction mixture and ultimately the salt is acidified [2][3][4]. These methods involve many steps for the work-up of the product. This problem was solved by the use of a mixture of acetone-benzene as the solvent for the direct separation of product. In this alternative method the product was crystallized directly from the sulfonation mixture using that solvent system. The advantages of this method are the fewer separation steps and the high yield (96%){lit [2] yield 95-96%}.

Scheme 1
Previous methods for the self-oxidation of 2 by sodium hypochlorite (Scheme 2) in aqueous solutions suffer from low yields and long reaction times [5][6][7][8]. By the use of diethylene glycol instead of water in this reaction we both increased the yield (from 86 to 93%) and reduced the reaction time.

Scheme 2
The above intermediate 3 can be converted into the triazinyl fluorescent brighteners 6 through the reduction of nitro groups to give 4, subsequent reaction with cyanuric chloride (5) and amines or alcohols (Scheme 3) [9,10].

Conclusions
A convenient method has been developed for the synthesis of 4-nitrotoluene-2-sulfonic acid and 4,4'-dinitrostilbene-2,2'-disulfonic acid as fluorescent brightener intermediates. Simple and clean workups, high yields and also short reaction times make this procedure an attractive method for the possible commercial synthesis of these products.

Acknowledgments
The authors gratefully acknowledge partial support of this work by the Research Affairs Office of The University of Kashan, Kashan, Iran. They also thank Mr. M. R. Halvagar for his help in submitting this paper.

General
Chemicals were purchased from the Fluka and Merck chemical companies. Melting points were taken on a Gallenkamp melting point apparatus and are uncorrected. 1 H-NMR spectra were obtained at 250 MHz using a Bruker Avance 250 NMR in DMSO-d 6 as the solvent. Mass spectra were obtained using a Finnigan Mat 8430 Mass spectrometer. The infrared spectra were determined on a Nicolet Magna series FTIR 550 spectrometer using KBr pellets. Thin layer chromatography (TLC) on commercial aluminium-backed plates of silica gel 60 F 254 was used to monitor the progress of the reactions.
Simplified method for the preparation of 4-nitrotoluene-2-sulfonic acid (2). 4-Nitrotoluene (13.7g, 0.1 mol) was melted at 55 ○ C and stirred in a 100 mL round-bottom flask during the dropwise addition of 24% oleum (21 mL, 0.4 mol). The temperature was then raised to 75 ○ C and stirring was continued at this temperature for one hour. When the sulfonation was complete (checked by TLC), the mixture was cooled and slowly added to water (50 mL) until the solid precipitated. The product (2) was filtered off and recrystallised from acetone-benzene (2:1) to give a cream colored solid melting at 133 ○ C {lit. [2]