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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73ee0bacab5a7576a6a3244747f6ea99
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01C3-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-2284
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01C3-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-22
filingDate 1960-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f924db7cad9b74a5ed8b365874177973
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dcba6730d4d8bd959c037facfc8cdc57
publicationDate 1963-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-931240-A
titleOfInvention Preparation of covalent isocyanates
abstract Covalent isocyanates of the formula M(NCO)n are prepared by refluxing a mixture of sodium cyanate or potassium cyanate with a covalent halide of formula MCln or MFn in an inert polar solvent or reaction medium, or in a mixture of an inert polar solvent or reaction medium with an inert non-polar solvent, subsequently separating precipitated sodium or potassium halide and fractionally distilling the liquid phase to remove solvent or medium. In the above formula M represents either one of the elements aluminium, lead, arsenic, antimony, vanadium, or iron, or one of the groups vanadyl, sulphuryl, thionyl and chromyl; and n represents the covalency of the element or group. When a mixed solvent is used, the polar solvent preferably constitutes 10-20% by weight of the whole solvent. Suitable non-polar solvents are benzene, paraffins, chlorohydrocarbons and ethers, while suitable polar solvents are nitriles (e.g. acetonitrile), ketones (e.g. acetone), esters (e.g. ethyl acetate), nitroparaffins and liquid sulphur dioxide. Specificatio 907,029 is referred to.
priorityDate 1960-04-25-04:00^^<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: 41.