1003045-91-7Relevant academic research and scientific papers
Synthesis and flame retardant potential of polyols based on bisphenol-S
Sonnenschein, Mark F.,Virgili, Justin M.,Babb, David A.,Bell, Bruce M.,Nickless, Brian C.
, p. 2102 - 2108 (2016/06/14)
Polyether polyols based on bisphenol-S were prepared by alkoxylation and compared with analogs based on bisphenol-A, as well as standard aromatic polyester, and polyether polyols for viscosity and temperature stability. Thermo-oxidative stability was determined by thermo-gravimetric analysis, pyrolysis gas chromatography/mass spectroscopy, and evolved gas analysis mass spectroscopy. Incorporation of the sulfone moiety was found to dramatically improve the thermo-oxidative stability of the neat polyol. Significant char formation was observed with gas phase evolution of flame retardant SO2 and aromatic sulfone only apparent at about 600 °C.
One-pot alkoxylation of phenols with urea and 1,2-glycols
Lin, Hsing-Yo,Dai, Shenghong A.
experimental part, p. 167 - 173 (2011/04/19)
A one-pot epoxide-free alkoxylation process has been developed for phenolic compounds. The process involves heating phenols and urea in 1,2-glycols at 170-190 °C using Na2CO3/ZnO as co-catalysts under atmospheric conditions. During the course of this new alkoxylation reaction, a five-membered ring cyclic carbonate intermediate, ethylene carbonate (EC) or propylene carbonate (PPC), was produced in-transit as the key intermediate and was subsequently consumed by phenols to form alkoxylated ether alcohols as final products in excellent yields. For instance, phenol, bisphenol A (BPA), hydroquinone and resorcinol were converted into their respective mono-alkoxylated ether alcohols on each of their phenolic groups in 80-95% isolated yields. In propoxylation of phenols, this approach shows great product selectivity favoring production of high secondary alcohols over primary alcohols in isomeric ratios of nearing 95/5. Since ammonia (NH3) and carbon dioxide (CO2) evolving from the reaction can be re-combined in theory into urea for re-use, the overall net-alkoxylation by this approach can be regarded as a simple condensation reaction of phenols with 1,2-glycols giving off water as its by-product. This one-pot process is simple, safe and environmentally friendlier than the conventional alkoxylated processes based on ethylene oxide (EO) or propylene oxide (PO). Moreover, this process is particularly well-suited for making short chain-length alkoxyether alcohols of phenols.
