TY - JOUR
T1 - "on-Water" Reaction of (Thio)isocyanate
T2 - A Sustainable Process for the Synthesis of Unsymmetrical (Thio)ureas
AU - Karche, Amit Dattatray
AU - Kamalakannan, Prabakaran
AU - Powar, Rajendra
AU - Shenoy, Gautham G.
AU - Padiya, Kamlesh J.
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/11/18
Y1 - 2022/11/18
N2 - We describe a facile, sustainable, and chemoselective process for the synthesis of unsymmetrical (thio)ureas through the "on-water"reaction of (thio)isocyanates with amines. Detailed mechanistic studies revealed that the physical nature and solubility of reagents in water are responsible for the observed reaction rate and selectivity. Significant efforts have been made to design a scalable process to achieve the "zero waste""water-mediated"protocol for the synthesis of (thio)ureas from (thio)isocyanates and amines. The decisive advantages of the process are the simple product isolation through filtration and the recycling of the water effluent. It also avoids the use of sensitive anhydrous reaction conditions and toxic volatile organic solvents. The developed process ensures that chemoselectivity and robustness and are successfully scaled-up to produce 100 g of isoproturon in high yield and purity. Green chemistry parameters such as process mass intensity, reaction mass efficiency, and molar efficiency values (with and without solvent) were calculated and compared.
AB - We describe a facile, sustainable, and chemoselective process for the synthesis of unsymmetrical (thio)ureas through the "on-water"reaction of (thio)isocyanates with amines. Detailed mechanistic studies revealed that the physical nature and solubility of reagents in water are responsible for the observed reaction rate and selectivity. Significant efforts have been made to design a scalable process to achieve the "zero waste""water-mediated"protocol for the synthesis of (thio)ureas from (thio)isocyanates and amines. The decisive advantages of the process are the simple product isolation through filtration and the recycling of the water effluent. It also avoids the use of sensitive anhydrous reaction conditions and toxic volatile organic solvents. The developed process ensures that chemoselectivity and robustness and are successfully scaled-up to produce 100 g of isoproturon in high yield and purity. Green chemistry parameters such as process mass intensity, reaction mass efficiency, and molar efficiency values (with and without solvent) were calculated and compared.
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U2 - 10.1021/acs.oprd.2c00266
DO - 10.1021/acs.oprd.2c00266
M3 - Review article
AN - SCOPUS:85141875923
SN - 1083-6160
VL - 26
SP - 3141
EP - 3152
JO - Organic Process Research and Development
JF - Organic Process Research and Development
IS - 11
ER -