In 1994,Bulletin de la Societe Chimique de France included an article by Berkous, Rabia; Dupas, Georges; Bourguignon, Jean; Queguiner, Guy. Recommanded Product: (3-Chlorophenyl)(phenyl)methanol. The article was titled 《Behavior and extension of the scope of NADH models to the reduction of non-activated ketones by a stable indolo NADH model compound in the presence of Lewis acids》. The information in the text is summarized as follows:
The reduction of non-activated ketones, e.g., acetophenone, by a very stable NADH model in the presence of Lewis acids (AlX3, Et2AlCl) is reported. During the reaction, a side equilibrated aldol condensation occurs. Due to the reversibility of this reaction, the overall yield in alc. is not notably diminished. The scope of NADH models has been extended for the first time to non-activated ketones, such as dialkyl, aryl alkyl and diaryl ketones. In the experimental materials used by the author, we found (3-Chlorophenyl)(phenyl)methanol(cas: 63012-03-3Recommanded Product: (3-Chlorophenyl)(phenyl)methanol)
(3-Chlorophenyl)(phenyl)methanol(cas: 63012-03-3) belongs to hydroxy-containing compounds. Hydroxy groups participate in the dehydration reactions that link simple biological molecules into long chains. The joining of a fatty acid to glycerol to form a triacylglycerol removes the −OH from the carboxy end of the fatty acid.Recommanded Product: (3-Chlorophenyl)(phenyl)methanol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts