In 2012,Advanced Synthesis & Catalysis included an article by Tian, Yu; Sui, Yi; Gu, Yonghong; Tian, Shi-Kai. Formula: C13H11ClO. The article was titled 《Expedient synthesis of functionalized triarylmethanols through tandem formation of geminal C-C and C-O bonds》. The information in the text is summarized as follows:
The rearrangement-oxidation of N,N-disubstituted anilines and the formal dehydrogenative cross-coupling of diarylmethanols with aniline derivatives were developed for the preparation of sym. and unsym. functionalized triarylmethanols. Both reactions proceed smoothly in trifluoroacetic acid in the presence of an inexpensive oxidant (MnO2 or K2S2O8) and a catalytic amount of Pd(AcO)2 to give a range of functionalized triarylmethanols in moderate to good yields and with extremely high regioselectivity. The two unprecedented reactions involve tandem formation of geminal C-C and C-O bonds, and they are synthetically useful, atom-efficient, and operationally simple. The experimental part of the paper was very detailed, including the reaction process of (3-Chlorophenyl)(phenyl)methanol(cas: 63012-03-3Formula: C13H11ClO)
(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.Formula: C13H11ClO
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts