Optimisation of the preparation and isolation of 5-amino-2,4,6-triiodoisophthalic acid dichloride

Autor: H.J.M. Gijsen, H.C.C.K. van Bakel, W. Zwaan, L.A. Hulshof
Přispěvatelé: Macromolecular and Organic Chemistry, Chemical Reactor Engineering
Jazyk: angličtina
Rok vydání: 1999
Předmět:
Zdroj: Organic Process Research & Development, 3(1), 38-43. American Chemical Society
ISSN: 1083-6160
Popis: A scaleable process for the chlorination of 5-amino-2,4,6-triiodoisophthalic acid to the corresponding acid chloride, a building block for the synthesis of iodinated X-ray contrast agents, has been developed. Two dimeric byproducts have been isolated and assigned structures consistent with an amide and an anhydride. Hydrolysis of the N-sulfinyl intermediate and simultaneous crystallisation of the phthalic acid chloride have been optimised by applying fractional factorial design.
Databáze: OpenAIRE