Polymeric alkylated 1,2 dihydroquinolines

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Mixing of two or more solid polymers; mixing of solid...

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546166, 525375, 525241, 260 4AR, C08F12606

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active

042476640

ABSTRACT:
Novel compounds formed by alkylating a polyvinyl aromatic resin with a substituted 1,2-dihydroquinoline (hereafter "TMDQ" for brevity), are found to be powerful stabilizers for organic materials subject to oxygen and heat degradation. As antioxidants these compounds are essentially non-bleeding and non-staining in rubber and polyolefins. Compositions comprising from about 0.1 to about 10.0 parts by weight of the novel compounds per 100 parts organic material, are found to be essentially stable for extended periods of time under normal conditions of use.
A process for alkylating a polyvinyl aromatic resin with TMDQ necessarily utilizes at least a stoichiometric quantity, with respect to TMDQ, of an anhydrous Friedel-Crafts type acid-acting metal halide catalyst in a solvent for the resin. The reaction is carried out at an elevated temperature preferably at about the boiling point of the solvent. Preselected ratios of TMDQ to the number of monomeric vinyl aromatic moieties in the resin, yield an alkylated reaction product with predetermined ratios of TMDQ moieties to polystyrene moieties.

REFERENCES:
Fieser et al., "Adv. Organic Chemistry", p. 635, Reinhard, New York, N. Y., 1961.

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