Samenvatting
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.
Originele taal-2 | Engels |
---|---|
Pagina's (van-tot) | 38-43 |
Aantal pagina's | 7 |
Tijdschrift | Organic Process Research & Development |
Volume | 3 |
Nummer van het tijdschrift | 1 |
DOI's | |
Status | Gepubliceerd - 1999 |