http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-406847-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_315ae544538aaeac6d1f4eed6754e4bb
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C43-1782
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D319-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-178
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P13-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-06
filingDate 1972-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1976-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-406847-A1
titleOfInvention PROCEDURE FOR OBTAINING SUBSTITUTE DIOXANS WITH HERBICIDAL EFFECT.
abstract Procedure for obtaining herbicidal-effect substituted dioxanes of general formula: **(See formula)** where R is hydrogen, alkyl, haloalkyl, cyanoalkyl, aryl, aryloxyalkyl, arylalkoxyalkyl or alkoxyalkyl, where any alkyl or substituted alkyl radical contains from 1 to 6 carbon atoms and any aryl radical is unsubstituted phenyl, furyl or thienyl or bearing a single X substituent defined as F, Cl, Br, lower alkyl, lower alkoxy, or benzyloxy; R2a is hydrogen or methyl and R2a and R2a together can represent two or more methylenes groups and thus form a spiral structure; R5 is hydrogen, alkyl, chloroalkyl or bromoalkyl, said alkyl groups containing from 1 to 4 carbon atoms; Rr is a phenyl, furyl, thienyl or monovalent aromatic pyridyl unsubstituted or having one, two or three Y substituents, defined as F, Cl, Br, CN, CF3, lower alkyl, or lower alkoxy, assuming that when Rr where unsubstituted phenyl and R2a is hydrogen and R5 is hydrogen or methyl, then R2 is a radical other than unsubstituted phenyl; characterized by: (a) either (1) substituted 5-hydroxy-1,3-dioxane, **(See formula)** in a solvent with sodium hydride to form the corresponding sodium alcoholate which is then reacted with arylmethyl chloride or bromide, Rr-CH2-Cl or Rr-CH2-Br, or (2) 2-arylmethoxy-1,3 is reacted -propanediol, Rr-CH2-O-OH (CH2OH) 2 with a carbonyl compound, R2 R2a C = O, in the presence of an acid catalyst; and (b) the product is separated from the reaction mixture. (Machine-translation by Google Translate, not legally binding)
priorityDate 1971-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID259
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID78475
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393636
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394843
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448056355
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393818
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419882314
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24758
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559553
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5360545
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559212

Total number of triples: 32.