1931
DOI: 10.1002/jlac.19314880115
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Farbstoffstudien in der Thionaphtenreihe

Abstract: Die Synthese des Thioindigos ist fur das Gesamtgebiet der indigoiden Kupenfarbstoffe der Ausgangspunkt gewesen und es ist im Laufe einer verhaltnismaljig kurzen Zeitspanne gelungen, an Stelle der Indolreste in vielfaltiger Weise Reste des Thionaphtens zu verwenden. Es ist bemerkenswert, da13 bisher noch nicht versucht wurde, die Chemie der Anthrachinon-Kupenfarbstoffe in ahnlicher Weise zu beeinflussen. Ersetzt man im Anthrachinon einen Benzolrest durch denThiophenrest, so erhalt man das Thiophanthrenchinon (I… Show more

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Cited by 26 publications
(2 citation statements)
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“…44 : mp 111 • C), which could be used in the next step without further purification. IR: 1690 (C O 45 (3.5 g, 0.017 mol) was dissolved in AcOH (100%, 120 mL). A solution of Br 2 (5.3 g, 0.033 mol) in AcOH (10 mL) was added.…”
Section: Preparationsmentioning
confidence: 99%
“…44 : mp 111 • C), which could be used in the next step without further purification. IR: 1690 (C O 45 (3.5 g, 0.017 mol) was dissolved in AcOH (100%, 120 mL). A solution of Br 2 (5.3 g, 0.033 mol) in AcOH (10 mL) was added.…”
Section: Preparationsmentioning
confidence: 99%
“…Schonberg, Petersen, and Kaltschnitt (2) reported the synthesis of thianaphthene-2-carboxylic acid by reacting thianaphthene with powdered sodium in anhydrous ether, followed by carbonation. Mayer, et al (3), described the synthesis of thianaphthene-2-carboxylic acid from omercaptobenzaldehyde and chloroacetic acid. I n 1950 Shirley and Cameron (4) described the synthesis of the 2-carboxylic acid by metalation of thianaphthene with n-butyllithium to form 2-thianaphthenyllithium which was then converted into the desired acid by carbonation and acidification.…”
mentioning
confidence: 99%