Iron-Catalyzed Alkyne-Based Multicomponent Synthesis of Pyrimidines under Air was written by Mondal, Rakesh;Chakraborty, Gargi;Guin, Amit Kumar;Sarkar, Susmita;Paul, Nanda D.. And the article was included in Journal of Organic Chemistry in 2021.SDS of cas: 1777-82-8 This article mentions the following:
An iron-catalyzed sustainable, economically affordable, and eco-friendly synthetic protocol for the construction of various trisubstituted pyrimidines I (R = Ph, cyclopropyl, 2-thienyl, etc.; R1 = Ph, cyclopropyl, 2-thienyl, etc.; R2 = H, NH2, Me, Ph, etc.) is described. A wide range of trisubstituted pyrimidines were prepared using a well-defined, easy to prepare, bench-stable, and phosphine-free iron catalyst featuring a redox non-innocent tridentate arylazo pincer under comparatively mild aerobic conditions via dehydrogenative functionalization of alcs. RCH2OH with alkynes R1CCH and amidines R2C(=NH)NH2. In the experiment, the researchers used many compounds, for example, (2,4-Dichlorophenyl)methanol (cas: 1777-82-8SDS of cas: 1777-82-8).
(2,4-Dichlorophenyl)methanol (cas: 1777-82-8) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.SDS of cas: 1777-82-8
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts