Abstract
AbstractNew monomers containing aldehyde groups in the alcohol component of methacrylates were prepared. The structure of these monomers prevents undesired spontaneous intramolecular cyclization reactions of pendant aldehyde groups of the corresponding polymers. 2,2‐Diethoxyethyl methacrylate (1) and its saturated analog, 2,2‐diethoxyethyl pivalate (3) and 3,3‐diethoxypropyl methacrylate (2) were prepared. The conditions for a selective hydrolysis of the acetal function of these compounds, leading to the corresponding aldehydes, were studied.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
