http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SE-9704190-L

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d7fe151308388476e056181c18272ea4
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C227-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-18
filingDate 1997-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b7d9e90498dff0425152759aac535cf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28e562cd29063502f67e9df264fb3d56
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publicationDate 1997-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SE-9704190-L
titleOfInvention Process for Preparation of 5-Amino-2,4,6-triiododisophthalic acid dichloride by chlorination with thionyl chloride in the presence of a catalyst
abstract A process for the preparation of 5-amino-2,4,6-triiodoisophthalic acid dichloride by chlorination of 5-amino-2,4,6-triiodoisophthalic acid with thionyl chloride in the presence of a suitable solvent characterized in that the reaction is carried out in the presence of catalytic amounts of a tetraalkylammonium salt of formula R1R2R3R4NX (I) wherein X is halogen, mesylate or tosylate; R1, R2, R3 and R4, the same or different, are C1-C20 alkyl groups so that the total number of carbon atoms of the groups R1, R2, R3 and R4 is higher than 16. The 5-amino-2,4,6-triiodoisophthalic acid dichloride obtained according to the process of the present invention is useful as intermediate in the synthesis of iodinated contrast media.
priorityDate 1995-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.