N-(2,5-Difluorobenzylidene)-1-(2,5-difluorobenzyl)methanimine

The conversion of 2,5-difluorobenzylamine to N-(2,5-difluorobenzylidene)-1-(2,5-difluorobenzyl)methanimine using an oxoammonium salt bearing the nitrate anion is reported. The reaction is operationally simple, and the product is obtained with good yield.

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Publication Details

Journal
Molbank
Published
2026-05-08
DOI
https://doi.org/10.3390/m2174
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

N-(2,5-Difluorobenzylidene)-1-(2,5-difluorobenzyl)methanimine

Tiffany L. Chen, Nicholas E. Leadbeater, Manisha Sharma
Molbank
Fluorine in Organic Chemistry
article

N-(2,5-Difluorobenzylidene)-1-(2,5-difluorobenzyl)methanimine

Tiffany L. Chen, Nicholas E. Leadbeater, Manisha Sharma
article en

Abstract

The conversion of 2,5-difluorobenzylamine to N-(2,5-difluorobenzylidene)-1-(2,5-difluorobenzyl)methanimine using an oxoammonium salt bearing the nitrate anion is reported. The reaction is operationally simple, and the product is obtained with good yield.

MolbankVol. 2026(3)
University of Connecticut (US)
University of Connecticut
Clean water and sanitation
Openalex Percentile: Top 8%
Fluorine in Organic Chemistry
DOIOpen Access PDFOpenAlex
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N-(2,5-Difluorobenzylidene)-1-(2,5-difluorobenzyl)methanimine — Tiffany L. Chen, Nicholas E. Leadbeater, et al. · Molbank (2026) | TGRS Research Map | TGRS