Cure of secondary carbamate groups by melamine-formaldehyde resins was written by Higginbottom, H. P.;Bowers, G. R.;Ferrell, P. E.. And the article was included in Journal of Coatings Technology in 1999.Synthetic Route of C9H20O2 The following contents are mentioned in the article:
Crosslink densities of films prepared from oligomeric urethane polyols suggested that the methoxymethyl groups of melamine-formaldehyde resins (I) could react with urethane groups (i.e., secondary carbamate groups) as well as reacting with hydroxyl groups. Co-reactants that contain secondary carbamate groups and no hydroxyl groups have been prepared with several types of backbone structures. Cure of such co-reactants by I resins has been studied using a gradient oven with determination of impact resistance, solvent resistance, and hardness. Several formulations from these cure profile sets have been selected for crosslink d. determinations by dynamic mech. anal. Crosslink densities of cured films are consistent with complete conversion of secondary carbamate groups at temperatures only slightly higher than those used for cure of hydroxyl groups. The -OH groups on certain acrylic polyols were converted to secondary carbamate groups. The original acrylic and the converted acrylic were both cured with I resins. Acid resistance was much better for films prepared from the acrylic that contained secondary carbamate groups. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Synthetic Route of C9H20O2).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Synthetic Route of C9H20O2
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts