Polyorthoesters for low-VOC coatings was written by Isaka, Hisashi;Yonehara, Yoichi. And the article was included in Proceedings of the Annual Meeting Technical Program of the FSCT in 2001.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:
A series of new oligomeric polyorthoesters for low-VOC coatings was prepared by protecting OH groups with orthoester compounds to achieve both low viscosity and excellent compatibility with crosslinking agents. These new oligomeric polyorthoesters were synthesized through co-condensation reaction among polyol, orthoester, and α or β – glycol compounds under an acidic condition. Here, the α or β- glycol compounds were used as stoppers to prevent excessive polymerization The polyorthoesters can easily be hydrolyzed with atm. moisture, and the reproduced OH groups can react with appropriate crosslinking agents. It is unique in this system that even the stoppers, α or β – glycol compounds, can react with the crosslinking agents to achieve an extremely low VOC emission. The polyorthoesters cured with polyisocyanate compounds proved to be highly cross-linked polymers showing excellent mech. properties, chem. resistance, etc. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Name: 2-Butyl-2-ethylpropane-1,3-diol).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Name: 2-Butyl-2-ethylpropane-1,3-diol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts