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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-71
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-71
filingDate 1972-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8670a3fff94f56f23a248ba43bb91a47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_567d97e551071391e7195c7633c3296c
publicationDate 1974-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2249372-A1
titleOfInvention PROCESS FOR THE PRODUCTION OF HIGHER MOLECULAR ALPHA, BETA-UNSATABLED ALDEHYDE
abstract The prepn. of high-molecular aldehydes (I) by the reaction of II with III: R9-CR8=CR7-CR5R6-CR3R4-CR2=CR1-CHO (I) R9-CR5=CR7-CR5R6-OR10 (II) C(H)R3R4-CR2=CR1-CHO (III) is carried out at increased temp. and between normal press. and 250 atmos. excess, in liquid phase. In the formulae, R1 and R2 are H, 1-4C alkyl or (alkyl-substd.) phenyl, R3, R5 and R7 are H or 1-4C alkyl, R4 is H or an (un)satd., (un)branched 1-12C (cyclo)aliphatic gp., R8 is 1-4C alkyl or, if R9 is phenyl, is H, R9 is an (un)branched, (un)satd. 1-12C (cyclo)aliphatic gp. in which C-C bonds may be interrupted by O or -O-CO-, or may be (alkyl-substd.) phenyl, and R10 is H or the acyl residue from a 1-5C carboxylic acid. I are raw materials for natural prods. and perfumes, e.g. beta-ionone, farnesol and phytol.
priorityDate 1972-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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