96424-44-1Relevant articles and documents
A Direct Method for the Efficient Synthesis of Benzylidene Acetal at Room Temperature
Reddy, Narra Rajashekar,Kumar, Rashmi,Baskaran, Sundarababu
supporting information, p. 1548 - 1552 (2019/01/09)
For the first time, a metal-free direct method has been developed for the efficient synthesis of benzylidene acetal at room temperature using Dowex 50WX8 as a solid acid catalyst and Cl3CCN as a novel water scavenger. At room temperature, a wide variety of aryl and α,β-unsaturated aldehydes react readily with functionalized 1,2- and 1,3-diols to furnish the corresponding acetals in very good yields. Labile functional groups, like N-Boc, N-Cbz, -OTBDMS, -OBn, -N3 and acetonide are found to be stable under the reaction conditions. The versatility of this method is further demonstrated with carbohydrate substrates and optically active diols.
Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions
Aliyan, Hamid,Fazaeli, Razieh,Massah, Ahmad Reza,Momeni, Ahmad Reza,Naghash, Hamid Javaherian,Moeinifard, Behzad
experimental part, p. 873 - 876 (2012/04/05)
Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.
Cadmium iodide catalyzed and efficient synthesis of acetals under microwave irradiations
Laskar, Dhrubojyoti Dey,Prajapati, Dipak,Sandhu, Jagir S.
, p. 1283 - 1284 (2007/10/03)
A new selective method of acetalization of aldehydes and ketones with 1,2-diols, 1,3-diols or alcohols mediated by cadmium iodide under microwave irradiation is achieved in excellent yields.
