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  4. Dimerization of 3-Chlorooxindoles Mediated by Potassium Ethyl­xanthate: Synthesis of Isoindigos
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Dimerization of 3-Chlorooxindoles Mediated by Potassium Ethyl­xanthate: Synthesis of Isoindigos

Author(s)
Meesin, Jatuporn
Chotsaeng, Nawasit
Kuhakarn, Chutima
Date Issued
August 17, 2022
Type
Article
DOI
10.1055/a-1784-2304
Abstract
A novel dimerization of 3-chlorooxindoles promoted by potassium ethylxanthate to access isoindigo derivatives is described. The reactions proceeded readily at room temperature in short reaction times. A mechanistic study revealed that the 3-chlorooxindole is initially converted into O-ethyl S-(2-oxo-2,3-dihydro-1H-indol-3-yl) dithiocarbonate, which subsequently undergoes dimerization with elimination of arbon disulfide. In almost all cases, analytically pure isoindigos were isolated in moderate to good yields without a requirement for chromatographic purification.
Citation
Synlett, 33(14), 1317-1322, 2022
Subjects

carbon disulfide

chlorooxindoles

dimerization

isoindigos

potassium ethylxantha...

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