Iron-Mediated N-Nitrosation of Secondary Amines under Ambient Conditions via a Nitrate Reduction Strategy

An efficient protocol for the synthesis of N-nitrosamines from secondary amines was developed utilizing iron(III) nitrate and sodium metabisulfite. The transformation proceeds via a nitrate-reduction strategy at room temperature in acetonitrile, affording N-nitrosamine products in good to excellent yields (75-93%). This methodology offers improved operational safety, faster reaction times, and a broad substrate scope.

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Publication Details

Journal
Synlett
Published
2026-08-20
DOI
https://doi.org/10.1055/a-2942-9172
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Iron-Mediated N-Nitrosation of Secondary Amines under Ambient Conditions via a Nitrate Reduction Strategy

Jeyakumar Kandasamy, Sruthi S Nair, Ravindra Sundaresan
Synlett
Chemical Synthesis and Reactions
article

Iron-Mediated N-Nitrosation of Secondary Amines under Ambient Conditions via a Nitrate Reduction Strategy

Jeyakumar Kandasamy, Sruthi S Nair, Ravindra Sundaresan
article en

Abstract

An efficient protocol for the synthesis of N-nitrosamines from secondary amines was developed utilizing iron(III) nitrate and sodium metabisulfite. The transformation proceeds via a nitrate-reduction strategy at room temperature in acetonitrile, affording N-nitrosamine products in good to excellent yields (75-93%). This methodology offers improved operational safety, faster reaction times, and a broad substrate scope.

Synlett
Pondicherry University (IN)
Openalex Percentile: Top 18%
Chemical Synthesis and Reactions
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