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Related Experiment Video

Updated: Jun 5, 2026

Preparation of N-(2-alkoxyvinyl)sulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines

Preparation of N-(2-alkoxyvinyl)sulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines

Published on: January 3, 2018

N-(2-Methoxy-ethyl)phthalimide.

Yoke Leng Sim¹, Azhar Ariffin, Seik Weng Ng

¹Department of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia.

Acta Crystallographica. Section E, Structure Reports Online

|January 5, 2011

Summary

The phthalimide derivative C(11)H(11)NO(3) was analyzed using X-ray crystallography. Its molecular structure reveals a unique crystallographic mirror plane, impacting its chemical properties and potential applications.

Area of Science:

Crystallography
Organic Chemistry
Molecular Structure Analysis

Background:

Phthalimide derivatives are important in medicinal chemistry and materials science.
Understanding the precise molecular geometry is crucial for predicting chemical behavior.

Purpose of the Study:

To elucidate the crystal structure of the novel molecule C(11)H(11)NO(3).
To identify key structural features, including symmetry elements and atomic arrangements.

Main Methods:

Single-crystal X-ray diffraction was employed to determine the three-dimensional structure.
Crystallographic data were analyzed to identify the molecular conformation and symmetry.

Main Results:

The molecule C(11)H(11)NO(3) crystallizes with a specific orientation.

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A crystallographic mirror plane bisects the phthalimide unit and includes specific atoms of the 2-methoxy-ethyl group.

This symmetry element influences the overall molecular architecture.

Conclusions:

The determined crystal structure provides fundamental insights into the molecular geometry of this phthalimide derivative.
The presence of the mirror plane is a significant characteristic that may influence intermolecular interactions and solid-state properties.