3,4-Cyanomethyl substituted thiophenes reacted with thionyl chloride in the presence of base to give dicyano substituted thieno(3,4-c)thiophenes. The use of selenium oxychloride furnished the corresponding cyano substituted seleno(3,4-c)thiophene. 1,2-Phenylenediacetonitriles gave the corresponding cyano substituted benzo(c)thiophenes and benzo(c)selenenophenes, respectively, upon reaction with thionyl chloride and selenium oxychloride in the presence of base.
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http://dx.doi.org/10.1021/jo010858m | DOI Listing |
Chem Commun (Camb)
December 2024
University of Turin - Department of Chemistry, Via Giuria 7, 10125, Turin, Italy.
The chemoselective synthesis of trisubstituted alkenyl halides (Cl, Br, F, I) starting from ketones and aldehydes and lithium halocarbenoids is reported. Upon forming the corresponding tetrahedral intermediate adduct, followed by the addition of thionyl chloride, a selective E2-type elimination is triggered, furnishing the targeted motifs. The transformation takes place under full chemocontrol: various sensitive functionalities ( ester, nitrile, nitro, or halogen groups) can be placed on the starting materials, thus documenting a wide reaction scope, as well as the application of the technique to biologically active substances.
View Article and Find Full Text PDFACS Appl Mater Interfaces
November 2024
Key Laboratory of Applied Surface and Colloid Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Institute of New Concept Sensors and Molecular Materials, Shaanxi Normal University, Xi'an, Shaanxi 710119, People's Republic of China.
Lithium thionyl chloride (Li-SOCl) batteries are widely used due to their high energy density and long shelf life. However, the corrosive nature of SOCl poses a safety hazard, necessitating effective leak detection methods. We report an approach for real-time fluorescent detection of SOCl leakage in Li-SOCl batteries using a tetraphenylethene-based nanofilm.
View Article and Find Full Text PDFJACS Au
August 2024
Flow Chemistry Group, Van't Hoff Institute for Molecular Sciences (HIMS), University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.
Herein, we report an approach for generating thionyl fluoride (SOF) from the commodity chemicals thionyl chloride (SOCl) and potassium fluoride (KF). The methodology relies on a microfluidic device that can efficiently produce and dose this toxic gaseous reagent under extremely mild and safe conditions. Subsequently, the in situ-generated thionyl fluoride is reacted with an array of structurally and electronically differing carboxylic acids, leading to the direct and efficient synthesis of highly sought-after acyl fluorides.
View Article and Find Full Text PDFBMJ Case Rep
July 2024
Burns & Plastic Surgery, Queen Elizabeth Hospital, Birmingham, UK.
There is an increasing trend globally of fire incidents as a direct consequence of battery failures[1-6], but a dearth of reporting in medical literature regarding injuries associated with primary lithium cell explosions. We present the case of an electrical engineer referred to the burns team as a chemical burn secondary to a D-cell lithium battery explosion. Initial assessment revealed an entry wound on the anteromedial thigh leaking contaminated fluid.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2024
Universität Bielefeld, Fakultät für Chemie, Centrum für Molekulare Materialien, Universitätsstraße 25, 33615, Bielefeld, Germany.
Although the adduct of aluminum trichloride with thionyl chloride has been reported, no thionyl chloride adduct of a main group element Lewis acid or organometallic compound has been structurally characterized. In this communication we present the synthesis and reactivity of the structurally ascertained adduct of thionyl chloride with tris(pentafluoroethyl)gallane as a representative of a main group element Lewis acid. Gallium and indium compounds with electron withdrawing groups, e.
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