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US 5,182,389 AGranted
Process for the preparation of 2-(2',4'-dihydroxyphenyl)-4,6-diaryl-s-triazines
AssigneeCiba-Geigy Corporation
InventorKurt Burdeska
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AssigneeCiba-Geigy Corporation
InventorKurt Burdeska
Estimating the term…
There is disclosed a process for the preparation of 2-(2', 4'-dihydroxyphenyl)-4,6-diaryl-s-triazines of formula ##STR1## which comprises reacting 2-hydroxy-4,6-diaryl-s-triazines of formula ##STR2## in the temperature range from 100.degree.-150.degree. C. with thionyl chloride in the presence of a catalytic amount of a polar solvent, and subsequently reacting the chloro-s-triazine intermediate with 1,3-dihydroxybenzene using a Lewis acid in the presence of an inert organic solvent, in which formulae (1) and (2) above the rings A may be further substituted by halogen, hydroxy, lower alkyl, lower alkoxy or lower alkoxycarbonyl. The process of the invention makes it possible to prepare in simple manner and in good yield 2-(2',4'-dihydroxphenyl)-4,6-diaryl-s-triazines which find utility as UV absorbers or as starting materials of the preparation of UV absorbers.
A process for the preparation of a 2-hydroxy-4,6-diaryl-s-triazine of formula (2), which comprises reacting an aqueous alkaline solution of a benzamidine hydrohalide in the temperature range from 0.degree. to 80.degree. C. with an alkyl halocarbonate to an alkyl benzimidoylcarbamate, adding an inert organic solvent to the resultant emulsion, and reacting the organic phase containing the alkyl benzimidoylcarbamate to give the 2-hydroxy-4,6-diaryl-s-triazine according to the reaction scheme ##STR10## wherein Hal.sub.1 and Hal.sub.2 are halogen and R is C.sub.1 -C.sub.4 alkyl, and the rings A may be further substituted by halogen, hydroxy, lower alkyl, lower alkoxy or lower alkoxycarbonyl.
Dependencies are inferred from the claim text.