Synthesis p. 482 - 483 (1988)
Update date:2022-07-29
Topics: Synthesis Column chromatography Melting point Yield Catalyst Solvent reflux Nucleophilic substitution Stirring TLC (thin-layer chromatography) NMR (nuclear magnetic resonance) Workup Purity IR (Infrared Spectroscopy) Acyl chloride
Tanabe, Yoo
Sanemitsu, Yuzuru
3-Chloromethyl-2(3H)-benzothiazolones 4 were synthesized from 1,3,5-triphenyl-1,3,5-triazines 2 and chlorocarbonylsulfenyl chloride in a one-pot procedure.The chlorine atom in 4 was substituted by three types of nucleophiles, namely, potassium acetate, p-
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Doi:10.1055/s-0029-1216636
(2009)Doi:10.1021/jo00260a014
(1988)Doi:10.1055/s-0028-1088110
(2009)Doi:10.1039/b822170g
(2009)Doi:10.1021/acs.orglett.7b03296
(2017)Doi:10.1002/chem.200802677
(2009)
