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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-56
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 2000-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce6d67c3361c94d509c7f035189fcbb4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efaba283c16d9047260f111ffb55bc26
publicationDate 2002-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1235775-A1
titleOfInvention Method for isomerising allyl alcohols
abstract The invention relates to a method for isomerising educt allyl alcohols to product allyl alcohols in the presence of tungsten oxo (VI) complexes, containing ligands which contain additional oxygen at temperatures of between 50 and 300 DEG C. Said method is characterised in that amino alcohols, such as triethanolamine, diethanolamine, monoethanolamine, tripropanolamine, dipropanolamine, 3-amino-1-propanol, 1-amino-2-propanol, 2-amino-1-propanol, butyldiethanolamine, methyldiisopropanolamine, N, N'-bis-(2-hydroxy-benzyl)-1,2-diaminoethane or N-(2-hydroxy-benzyl)-amine are contained in the catalyst as ligands which contain additional oxygen, in addition to the oxygen bases known as ligands containing additional oxygen or in place of these oxygen bases. The method is particularly suitable for producing tertiary product allyl alcohols, such as linalool, by isomerising primary or secondary allyl alcohols such as geraniol and nerol.
priorityDate 1999-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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