The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
Feb. 02, 1988
Filed:
Dec. 08, 1986
Charles E Monnier, Villars-sur-Glane, CH;
Friedrich Stockinger, Courtepin, CH;
Ciba-Geigy Corporation, Ardsley, NY (US);
Abstract
A process for the preparation of glycidyl compounds by reacting a compound containing at least one phenolic group with at least the equivalent amount, based on the phenolic group, of a halohydrin in a substantially anhydrous, aprotonic solvent in the presence of a solid, substantially anhydrous catalyst, is described, which process comprises carrying out the reaction at a temperature in the range from 40.degree. to 80.degree. C. in the presence of an alkali metal carbonate, an aprotonic dipolar solvent with a static relative dielectric constant of more than 25 (at 25.degree. C.) and a permanent electric dipole moment of more than 2.5 D being used, an additional feature of said solvent being that the transition energy of the solvatochromic absorption band of the dissolved N-(3,5-diphenyl-4-hydroxyphenyl)-2,4,6-triphenylpyridinium perchlorate is in the range from 168 to 197.4 kJ/mole (at 25.degree. C.), or which process comprises carrying out the reaction at a temperature in the range from 60.degree. to 80.degree. C. in the presence of an alkali metal hydroxide and a phase transfer catalyst chosen from the group consisting of ammonium and/or phosphonium compounds, the water of reaction formed being removed continuously and an inert, aprotonic, apolar solvent with a static relative dielectric constant of less than 8.0 (at 25.degree. C.) and a permanent electric dipole moment of less than 2.0 D being used, an additional feature of said solvent being that the transition energy of the solvatochromic absorption band of the dissolved N-(3,5-diphenyl-4-hydroxyphenyl)-2,4,6-triphenylpyridinium perchlorate is in the range from 140 to 165 kJ/mole (at 25.degree. C.). The resins obtained in this manner have a high degree of epoxidation and a low content of hydrolysable or ionic halogen. They are particularly suitable as potting resins for electronic components.