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Efficient Synthesis of a 2-Decyl-tetradecyl Substituted 7-Bromophenothiazine-3-carbaldehyde Building Block for Functional Dyes

Authors :
Burak Kürsat Börüsah
Thomas J. J. Müller
Source :
Organics, Vol 3, Iss 4, Pp 502-506 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

(1) Polyfunctional molecules are versatile building blocks for efficient syntheses of novel phenothiazine-based materials with promising electronic properties. A prerequisite is a facile, high yielding access to these building blocks that bear solubilizing moieties and functional groups for orthogonal transformation. (2) Here, an efficient, improved two-step protocol for accessing a solubilizing 2-decyl-tetradecyl functionalized phenothiazine, i.e., an N-alkylated 7-bromophenothiazine-3-carbaldehyde, by Vilsmeier–Haack formylation and NBS (N-bromo succinimide) bromination is reported. (3) The sequence proceeds with higher yields and in shorter reaction times than the standard access employing bromination with elementary bromine. In addition, the work-up procedure essentially uses absorptive filtration on a plug of silica with the eluent.

Details

Language :
English
ISSN :
2673401X
Volume :
3
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Organics
Publication Type :
Academic Journal
Accession number :
edsdoj.b263ed8b483b46bab80d99119520ec90
Document Type :
article
Full Text :
https://doi.org/10.3390/org3040033