Diaryl-2H-naphthopyrans
AssigneeOptische Werke G. Rodenstock
InventorsManfred Melzig, Herbert Zinner
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Abstract
Photochromic diaryl-2H-naphthopyran structures, which dye photochromically well at room temperature, lighten up quickly when incorporated into ophthalmic lenses, possess longevity, and due to their special structure, have a reduced tendency of the molecules to migrate in plastics.
Claims2
A photochromic substance having a diaryl-naphthopyran structures linked in the form Y—Ar—Y, Y—Ar—Y′, Y—Ar-Z, Z-Ar-Z or Z-Ar-Z′, with Y, Y′, Z and Z′ being pyrans.
A photochromic substance having a diaryl-naphthopyran structure, characterized by it possessing an aryl substituent which reduces the molecule migration in plastics, obtained by:
- a) Synthesis of a ketone from a diaryl alkane and/or a diarylether and a halogenated arylcarbonic acid by Friedel Crafts' acylation according to the following reaction diagram:
- R=H, F, Cl, Br, Phenyl, Benzyl, OR′, R′, NR′2
- R′=alkyl with up to 6 C-atoms or cycloalkyl with 5 or 6 C-atoms
- b) Synthesis of a tertiary alcohol having carbon-carbon-triple links from the ketone yielded by a) and a metal acetylide by means of nucleophilic addition.
- c) Synthesis of the photochromic substance by means of condensation of said tertiary alcohol with a substituted diarylalcohol according to the following reaction diagram:
- with:
- X,Ar,R,R′ as under a)
Dependencies are inferred from the claim text.