http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2714799-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-00
filingDate 1977-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_023aa5b5c17c9cb660e8c9d129086a54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33a424f64bdb5df5c36b6379b478a90b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce72e59844d1cd29b60c43a705408b74
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publicationDate 1978-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2714799-A1
titleOfInvention PROCESS FOR THE PRODUCTION OF 1,4-DICYANE BUTEN
abstract (I), prepn. by reaching butenediol esters, (II), with at least equiv. quantities of HCN at 60-160 degrees C., takes place in aq. solns. of CuBr contg. alkali bromide, under pressures >=2 (pref. 2-20) bar. Mol. ratio CuBr to (II) is (0.3-0.6) : 1. The alkali bromide is esp. NaBr. The aq. solns. pref. also contain NH4Br and up to 10 wt.% HBr. (I) can be hydrogenated to hexamethylene diamine, used in polyamide prodn. On replacing previously used CuCl + alkali halide by CuBr + alkali bromide, yields of (I) can be increased, e.g. from 30% to >80%. Process can be effected economically on a large scale. Aq. solns. are handled more easily than fused salts. (I) is easily separated.
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priorityDate 1977-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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