开发用于烯烃环氧化的纯可分离(二吗啉基)三嗪试剂

IF 1.7 4区 化学 Q3 CHEMISTRY, ORGANIC Synlett Pub Date : 2024-07-18 DOI:10.1055/a-2356-8451
Hikaru Fujita, Toshiyuki Kato, Tatsuki Betsuyaku, Munetaka Kunishima
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引用次数: 0

摘要

我们开发了一种基于三嗪的试剂--2-氢过氧-4,6-二吗啉基-1,3,5-三嗪(Triazox-II),用于烯环氧化反应。这种试剂可从廉价的起始材料(三聚氯氰和吗啉)中以 15 毫摩尔的规模分两步制备,总产率为 54%,分离出来的试剂是一种纯净、台式稳定的固体,对冲击和摩擦的敏感性较低。与之前报道的试剂 Triazox 相比,Triazox-II 在氯化溶剂中的溶解度更高。使用 Triazox-II 在各种溶剂中进行环氧化反应,首选 0.5 M 浓度的 CH2Cl2,生成的环氧化物收率为 83-94%。由于反应副产物的酸度较低,因此反应是在温和的条件下进行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Development of a Purely Isolable (Dimorpholino)triazine-Based Reagent for the Epoxidation of Alkenes

A triazine-based reagent, 2-hydroperoxy-4,6-dimorpholino-1,3,5-triazine (Triazox-II), was developed for alkene epoxidation. This reagent can be prepared from inexpensive starting materials (cyanuric chloride and morpholine) on a 15 mmol scale in two steps with 54% overall yield and isolated as a pure, bench-stable solid with low sensitivity to impact and friction. Triazox-II exhibited higher solubility in chlorinated solvents than the previously reported reagent Triazox. Epoxidation using Triazox-II was conducted in various solvents, with a preference for CH2Cl2 at 0.5 M concentration, resulting in epoxides in 83–94% yield. The reaction was conducted under mild conditions owing to the low acidity of the reaction coproduct.

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来源期刊
Synlett
Synlett 化学-有机化学
CiteScore
3.40
自引率
5.00%
发文量
369
审稿时长
1 months
期刊介绍: SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.
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