Department of Chemistry, North Caucasus Federal University, 1a Pushkin St., 355017 Stavropol, Russia.
Int J Mol Sci. 2024 Aug 11;25(16):8750. doi: 10.3390/ijms25168750.
A new variant of Fisher indole synthesis involving Bronsted acid-catalyzed hydrohydrazination of unactivated terminal and internal acetylenes with arylhydrazines is reported. The use of polyphosphoric acid alone either as the reaction medium or in the presence of a co-solvent appears to provide the required balance for activating the C-C triple bond towards the nucleophilic attack of the hydrazine moiety without unrepairable reactivity loss of the latter due to competing amino group protonation. Additionally, the formal hydration of acetylenes to the corresponding ketones occurs under the same conditions, making it an alternative approach for generating carbonyl groups from alkynes.
报道了一种涉及布朗斯特酸催化的未活化末端和内部炔烃与芳基腙的 hydrohydrazination 的费舍尔吲哚合成的新变体。单独使用多聚磷酸或者在共溶剂的存在下作为反应介质似乎提供了所需的平衡,以激活 C-C 三键,使其能够受到肼部分的亲核攻击,而不会由于后者的氨基质子化而导致不可修复的反应性损失。此外,在相同条件下,炔烃可正式水合生成相应的酮,因此这是一种从炔烃生成羰基的替代方法。