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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1ad50594922e91511cbca4322ddcae90
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C205-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-164
filingDate 1980-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_737f4010f100cf3a20dceb10e1617c0e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41565248bcdba117462a58a304f63402
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b03dbdda58cba0027c88c501219908d
publicationDate 1987-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SE-447989-B
titleOfInvention PROCEDURE FOR THE PREPARATION OF (2-METOXYETENYL) NITROBENZENES
abstract In the prepn. of 2 and 4 substit. alkoxy ethenyl benzenes and alkoxy ethyl benzenes, 0- or p- halonitrobenzene is reacted with at least an equiv. of alkyl ether in presence of a trialkylamine and a Pd catalyst. Pref. the catalyst is part. Pd acetate or Pd or carbon. The reaction is carried out at 80-140 pref. 100-120 deg.C. for 10-20 hrs. at pressure with equiv. quant. of pref. triethylanine or tributylamine. The pref. halogens are Br and I. Treatment of the initial reaction prod. with aqueous acid and triethanolamine to enable sepn. of the unwanted 2-aryl vinyl ether is also claimed. The method gives improved yield of intermediates in the synthesis of the beta blocker metoprolol. Provisional Basic previously advised in Week E23).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109553513-A
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priorityDate 1980-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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