结合 AlCl3 和 HFIP 对 N-苄氧羰基 (N-Cbz) 进行脱保护的温和方法

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC
Vinothkumar Vinayagam*, Subir Kumar Sadhukhan, Durga Varaprasad Botla, Rajashekar Reddy Chittem, Sreenivasa Reddy Kasu and Tanguturi Venkatanarayana Hajay Kumar, 
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引用次数: 0

摘要

在此,我们报告了氯化铝(AlCl3)在氟化溶剂 1,1,1,3,3,3-hexafluorisopropanol [HFIP] 中选择性地脱保护 N-苄氧羰基(N-Cbz)的新发现。该方法的显著特点是对包括其他可还原基团在内的官能团具有良好的耐受性、成本效益高、操作简便、方案安全、易于放大、产率高以及可在常温下进行反应。该方法是使用发火氢气和金属催化剂试剂的绝佳替代品,因为它们会带来严重的安全和环境问题。该方法最显著的特点是在有 O-和 N-Bn 保护基团存在的情况下对 N-Cbz 基团进行正交脱保护,从而扩大了设计合成路线的范围,以合成需要多个官能团转化的目标化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mild Method for Deprotection of the N-Benzyloxycarbonyl (N-Cbz) Group by the Combination of AlCl3 and HFIP

Mild Method for Deprotection of the N-Benzyloxycarbonyl (N-Cbz) Group by the Combination of AlCl3 and HFIP

Mild Method for Deprotection of the N-Benzyloxycarbonyl (N-Cbz) Group by the Combination of AlCl3 and HFIP

Herein, we report our findings on the novel ability of aluminum chloride (AlCl3) in fluorinated solvent 1,1,1,3,3,3-hexafluoroisopropanol [HFIP] to selectively deprotect the N-benzyloxycarbonyl group (N-Cbz). The salient features of this method are good functional group tolerance including other reducible groups, cost-effectiveness, easy-to-handle, safe protocol, amenable to scale-up, high yields, and ambient temperature reactions. The methodology would serve as an excellent alternative to the use of pyrophoric hydrogen gas and metal catalyst reagents that pose severe safety and environmental concerns. The most notable feature of this methodology is the orthogonal deprotection of the N-Cbz group in the presence of O- and N-Bn protecting groups, hence, expanding the scope for designing synthetic routes to target compounds requiring multiple functional group transformations.

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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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