Hexafluoroisopropanol Mediated Ring-Opening Reactions of Epoxides with Indoles Under Catalyst-Free Conditions

An efficient, catalyst-free, and room-temperature protocol has been developed for the ring-opening reactions of ring cyclic ethers with indoles in Hexafluoroisopropanol (HFIP). Under these mild conditions, a diverse range of indoles smoothly reacted with oxirane within 6 h, affording the corresponding C3-alkylated indoles in good-to-excellent yields. Notably, this method also shows promising reactivity toward four-membered oxetanes. Furthermore, stereospecific investigations employing enantiopure (R)-styrene oxide afforded the corresponding products with high enantiomeric excess, suggesting an SN2 pathway with inversion of configuration. The unique hydrogen-bonding ability and acidity of HFIP are crucial for driving this facile transformation. This protocol offers a green, atom-economical, and sustainable approach for constructing structurally diverse indole derivatives, showcasing high practical utility for organic synthesis.

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Publication Details

Journal
Molecules
Published
2026-09-04
DOI
https://doi.org/10.3390/molecules31173108
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Hexafluoroisopropanol Mediated Ring-Opening Reactions of Epoxides with Indoles Under Catalyst-Free Conditions

Murong Zhan, 马养民, Zhichao Wang, Ding Ma et al.
Molecules
Synthesis and Catalytic Reactions
article

Hexafluoroisopropanol Mediated Ring-Opening Reactions of Epoxides with Indoles Under Catalyst-Free Conditions

Murong Zhan, 马养民, Zhichao Wang, Ding Ma, Qian Jiao, Sen Yang
article en

Abstract

An efficient, catalyst-free, and room-temperature protocol has been developed for the ring-opening reactions of ring cyclic ethers with indoles in Hexafluoroisopropanol (HFIP). Under these mild conditions, a diverse range of indoles smoothly reacted with oxirane within 6 h, affording the corresponding C3-alkylated indoles in good-to-excellent yields. Notably, this method also shows promising reactivity toward four-membered oxetanes. Furthermore, stereospecific investigations employing enantiopure (R)-styrene oxide afforded the corresponding products with high enantiomeric excess, suggesting an SN2 pathway with inversion of configuration. The unique hydrogen-bonding ability and acidity of HFIP are crucial for driving this facile transformation. This protocol offers a green, atom-economical, and sustainable approach for constructing structurally diverse indole derivatives, showcasing high practical utility for organic synthesis.

MoleculesVol. 31(17)
Shaanxi University of Science and Technology (CN)
National Natural Science Foundation of China
Responsible consumption and production
Openalex Percentile: Top 20%
Synthesis and Catalytic Reactions
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