http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1116472-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C19-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-206
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C19-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-20
filingDate 1966-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9a5f146d90817ebbd3cce33895f959c
publicationDate 1968-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1116472-A
titleOfInvention Primary alkyl bromides and chlorides from alpha-olefins
abstract Primary alkyl bromides are prepared by selectively hydrobrominating a C6- 20 a -olefinic hydrocarbon with HBr in the presence of HCl at 0-100 DEG C. under anhydrous conditions, the reaction being initiated by free-radical catalysis. The primary alkyl bromides may be converted to the corresponding alky chlorides by passing dry HCl gas at 130-300 DEG C. into a solution of the alkyl bromide and lithium chloride or bromide or a quaternary ammonium chloride or bromide in an organic acid of the formula RCOOH, wherein R is an inert hydrocarbon radical containing less than 21 carbon atoms optionally having one or more hydrogen atoms replaced by F, Cl or Br. In the hydrobromination of dodecene-1 followed by reaction with HCl, the product contains dodecyl bromide and chloride, plus 1,12-dibromo-, 1,12-dichloro- and 1 - chloro - 12 - bromo - undecane resulting from 1,11-dodecadiene impurity in the dodecene feed.
priorityDate 1965-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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